Difference between revisions of "Task 5 - Mapping SNPs Canavan"

From Bioinformatikpedia
(Coding SNPs)
(Coding SNPs)
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MTSCHIAEEHIQKVAIFGGTHGNELTGVFLVKHWLENGAEIQRTGLEVKPFITNPRAVKKCTRYIDCDLNRIFDLENLGKKMSEDLPYEVRRAQEINHLF
 
  +
R G T R P G TR R A T A K T A
 
  +
MTSCHIAEEHIQKVAIFGGTHGNELTGVFLVKHWLENGAEIQRTGLEVKP 50
GPKDSEDSYDIIFDLHNTTSNMGCTLILEDSRNNFLIQMFHYIKTSLAPLPCYVYLIEHPSLKYATTRSIAKYPVGIEVGPQPQGVLRADILDQMRKMIK
 
r V Y D E V RYI T F I H T A T Hr F R
+
R G T R P G TR R
  +
HALDFIHHFNEGKEFPPCAIEVYKIIEKVDYPRDENGEIAAIIHPNLQDQDWKPLHPGDPMFLTLDGKTIPLGGDCTVYPVFVNEAAYYEKKEAFAKTTK
 
  +
FITNPRAVKKCTRYIDCDLNRIFDLENLGKKMSEDLPYEVRRAQEINHLF 100
S Er r T K r KN T R V T P R TMHLM AATF S
 
  +
A T A H T A
LTLNAKSIRCCLH-
 
  +
K
  +
GPKDSEDSYDIIFDLHNTTSNMGCTLILEDSRNNFLIQMFHYIKTSLAPL 150
  +
R V Y D E V
  +
E I F
  +
PCYVYLIEHPSLKYATTRSIAKYPVGIEVGPQPQGVLRADILDQMRKMIK 200
  +
RYI T F I H T A T HR F R
  +
W C L
  +
HALDFIHHFNEGKEFPPCAIEVYKIIEKVDYPRDENGEIAAIIHPNLQDQ 250
  +
S ER X T K C KN T R V
  +
R T R L
  +
DWKPLHPGDPMFLTLDGKTIPLGGDCTVYPVFVNEAAYYEKKEAFAKTTK 300
  +
T P R TMHPM AATF S
  +
S D C
  +
LTLNAKSIRCCLH- 314
 
E G W
 
E G W

Revision as of 14:59, 8 June 2012

First impression

Protocol

Further information can be found in the protocol.

HGMD

74 (79 in 2012 professional) total for cDNA sequence NM_000049.2 and amino acid sequence NP_000040.1, out of which

  • 47 missense/nonsense
  • 5 splicing
  • 12 small deletions
  • 2 small insertions
  • 1 indel
  • 7 gross deletions

link to search

SNPdbe

  • 55 total, includes predicted functional effect. 29 of these 55 labelled as involved in Canavan Disease.

link to search

dbSNP

  • same identifiers for sequence as HGMD
  • "synonymous-codon"[Function_Class] AND ASPA[GENE] AND "human"[ORGN] AND "snp"[SNP_CLASS] yields only 9 results
  • 505 results for SNPs in general in human
    • 458 for NP_000040.1 (coding: 23)
    • 493 for NP_001121557.1 (coding: 23)

SNPedia

links to other pages

Coding SNPs

Residue PositionIdentifierReference DBValidation evidenceSNP TypeMutation
4rs142041344 dbSNP
SNPDBe

1000Genomes
missenseC4R
14CM063852HGMDZeng (2006) Mol Genet Metab 89missenseV14G
16
CM960084
SNPDBe
HGMD

Kaul (1996) Am J Hum Genet 59
missenseI16T
18CM067343HGMDZeng (2006) Adv Exp Med Biol 576missenseG18R
21
CM001608
SNPDBe
HGMD

Sistermans (2000) Eur J Hum Genet 8
missenseH21P
24rs104894551
CM023602
dbSNP
SNPDBe
OMIM
HGMD
Multiple independent submissions to the refSNP cluster
by cluster
Zeng (2002) J Inherit Metab Dis 25
missenseE24G
26rs145616193 dbSNPsynonymousT26T
27
CM960085
SNPDBe
HGMD

Kaul (1996) Am J Hum Genet 59
missenseG27R
33rs138158568 dbSNP
SNPDBe
missenseH33R
53rs17850703 dbSNP
SNPDBe
missenseT53A
57
CM001609
SNPDBe
HGMD

Sistermans (2000) Eur J Hum Genet 8
missenseA57T
68
CM023603
SNPDBe
HGMD

Zeng (2002) J Inherit Metab Dis 25
missenseD68A
71rs104894553
CM060201
dbSNP
SNPDBe
HGMD
multiple independent submissions to the refSNP cluster
by cluster
Janson (2006) Ann Neurol 59
missenseR71H
71_2SNPDBemissenseR71K
82rs80099330 dbSNP
SNPDBe
Multiple independent submissions to the refSNP cluster
Validated by frequency or genotype data
1000Genome project
1000Genomes
frequency
cluster
missenseM82T
93rs144639820 dbSNPValidated by frequency or genotype datasynonymousA93A
109CM990192HGMDElpeleg (1999) J Inherit Metab Dis 22nonsenseY109Ter
111rs181347986 dbSNP
SNPDBe
1000Genome project
1000Genomes
missenseI111V
114
CM023014
SNPDBe
HGMD

Olsen (2002) J Med Genet 39
missenseD114Y
114_2CM960086HGMDKaul (1996) Am J Hum Genet 59missenseD114E
121rs148451498 dbSNP
SNPDBe
missenseN121D
121_2CM063846HGMDZeng (2006) Mol Genet Metab 89missenseN121I
123
CM960087
SNPDBe
HGMD

Kaul (1996) Am J Hum Genet 59
missenseG123E
143_2CM063849HGMDZeng (2006) Mol Genet Metab 89missenseI143F
143rs199565861dbSNP
SNPDBe

1000Genomes
missenseI143V
152rs104894548
CM950102
dbSNP
SNPDBe
OMIM
HGMD
Multiple independent submissions to the refSNP cluster
by cluster
Kaul (1995) Hum Mutat 5
missenseC152R
152_2CM023604HGMDZeng (2002) J Inherit Metab Dis 25missenseC152W
153rs141755746 dbSNPsynonymousY153Y
154rs147193431
rs2228435
dbSNP
SNPDBe
missenseV154I
157rs140357187 dbSNP
SNPDBe
missenseI157T
164SNPDBemissenseY164F
166CM063847HGMDZeng (2006) Mol Genet Metab 89missenseT166I
168
CM001610
SNPDBe
HGMD

Sistermans (2000) Eur J Hum Genet 8
missenseR168H
168_2CM960089HGMDKaul (1996) Am J Hum Genet 59missenseR168C
170rs144321760 dbSNP
SNPDBe
Validated by frequency or genotype data
by freq
missenseI170T
178SNPDBemissenseE178A
181_2CM063850HGMDZeng (2006) Mol Genet Metab 89missenseP181L
181
CM001611
SNPDBe
HGMD

Sistermans (2000) Eur J Hum Genet 8
missenseP181T
183
CM990193
SNPDBe
HGMD

Elpeleg (1999) J Inherit Metab Dis 22
missenseP183H
184CM023605HGMDZeng (2002) J Inherit Metab Dis 25nonsenseQ184Ter
186
CM990194
SNPDBe
HGMD

Elpeleg (1999) J Inherit Metab Dis 22
missenseV186F
195
CM990195
SNPDBe
HGMD

Elpeleg (1999) J Inherit Metab Dis 22
missenseM195R
202rs147763700 dbSNP
SNPDBe
missenseA202S
213CM055097HGMDTacke (2005) Neuropediatrics 36missenseK213E
214CM023606HGMDZeng (2002) J Inherit Metab Dis 25nonsenseE214Ter
218rs104894549 dbSNP Multiple independent submissions to the refSNP clusternonsenseC218X
218_2CM950103HGMDShaag (1995) Am J Hum Genet 57nonsenseC218Ter
220rs139053885 dbSNP
SNPDBe
missenseI220T
226_2CM086530HGMDDi Pietro (2008) Clin Biochem 41missenseI226T
226rs201887670dbSNPmissenseI226K
231rs104894550
CM994594
dbSNP
SNPDBe
OMIM
HGMD
Multiple independent submissions to the refSNP cluster
by cluster
Rady (1999) Am J Med Genet 87
missenseY231C
231_2CM940123HGMDKaul (1994) Am J Hum Genet 55nonsenseY231Ter
235rs149842031 dbSNP
SNPDBe
Multiple independent submissions to the refSNP cluster
Validated by frequency or genotype data
1000Genome project
1000Genomes
frequency
cluster
missenseE235K
236rs149189911 dbSNPsynonymousN236N
239rs145085349 dbSNP
SNPDBe
missenseI239T
244
CM023607
SNPDBe
HGMD

Zeng (2002) J Inherit Metab Dis 25
missenseH244R
244_2CM063848HGMDZeng (2006) Mol Genet Metab 89missenseH244L
249rs104894552
CM023015
dbSNP
SNPDBe
HGMD
Multiple independent submissions to the refSNP cluster
by cluster
Olsen (2002) J Med Genet 39
missenseD249V
270rs200126822dbSNP
SNPDBe

1000Genomes
missenseI270T
272CM063851HGMDZeng (2006) Mol Genet Metab 89missenseL272P
274
CM950104
SNPDBe
HGMD

Shaag (1995) Am J Hum Genet 57
missenseG274R
277rs78677072 dbSNP Multiple independent submissions to the refSNP cluster
1000Genome project
synonymousT277T
278rs140581464 dbSNP
SNPDBe
Multiple independent submissions to the refSNP cluster
Validated by frequency or genotype data
1000Genome project
1000Genomes
frequency
cluster
missenseV278M
279rs145717248 dbSNP
SNPDBe
missenseY279H
280rs148081446 dbSNP Multiple independent submissions to the refSNP cluster
Validated by frequency or genotype data
1000Genome project
synonymousP280P
280_2CM990197HGMDElpeleg (1999) J Inherit Metab Dis 22missenseP280S
281rs141858640 dbSNP
SNPDBe
missenseV281M
285rs28940279
CM930046
dbSNP
SNPDBe
OMIM
HGMD
Multiple independent submissions to the refSNP cluster
Validated by frequency or genotype data
"by cluster
Kaul (1993) Nat Genet 5
missenseE285A
285_2SNPDBemissenseE285D
286rs138062143 dbSNPsynonymousA286A
287
CM990198
SNPDBe
HGMD

Elpeleg (1999) J Inherit Metab Dis 22
missenseA287T
288SNPDBemissenseY288F
288_2CM034717HGMDSurendran (2003) Mol Genet Metab 80missenseY288C
295
CM950105
SNPDBe
HGMD

Shaag (1995) Am J Hum Genet 57
missenseF295S
305rs28940574
CM940124
dbSNP
SNPDBe
OMIM
HGMD
Multiple independent submissions to the refSNP cluster
by cluster
Kaul (1994) Am J Hum Genet 55
missenseA305E
310SNPDBemissenseC310G
314CM023608HGMDZeng (2002) J Inherit Metab Dis 25missenseTer314W



MTSCHIAEEHIQKVAIFGGTHGNELTGVFLVKHWLENGAEIQRTGLEVKP  50
   R         G T R  P  G TR     R                 
                                                  
FITNPRAVKKCTRYIDCDLNRIFDLENLGKKMSEDLPYEVRRAQEINHLF  100
  A   T          A  H          T          A       
                    K                             
GPKDSEDSYDIIFDLHNTTSNMGCTLILEDSRNNFLIQMFHYIKTSLAPL  150
        R V  Y      D E                   V       
             E      I                     F       
PCYVYLIEHPSLKYATTRSIAKYPVGIEVGPQPQGVLRADILDQMRKMIK  200
 RYI  T      F I H T       A  T HR F        R     
 W               C            L                   
HALDFIHHFNEGKEFPPCAIEVYKIIEKVDYPRDENGEIAAIIHPNLQDQ  250
 S          ER   X T     K    C   KN  T    R    V 
                 R       T    R            L      
DWKPLHPGDPMFLTLDGKTIPLGGDCTVYPVFVNEAAYYEKKEAFAKTTK  300
                   T P R  TMHPM   AATF      S     
                             S    D  C            
LTLNAKSIRCCLH-  314
    E    G   W