Task 5 - Mapping SNPs Canavan
From Bioinformatikpedia
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
SNPdbe
- 55 total, includes predicted functional effect. 29 of these 55 labelled as involved in Canavan Disease.
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 Position | Identifier | Reference DB | Validation evidence | SNP Type | Mutation |
4 | rs142041344 | dbSNP SNPDBe | 1000Genomes | missense | C4R |
14 | CM063852 | HGMD | Zeng (2006) Mol Genet Metab 89 | missense | V14G |
16 | CM960084 | SNPDBe HGMD | Kaul (1996) Am J Hum Genet 59 | missense | I16T |
18 | CM067343 | HGMD | Zeng (2006) Adv Exp Med Biol 576 | missense | G18R |
21 | CM001608 | SNPDBe HGMD | Sistermans (2000) Eur J Hum Genet 8 | missense | H21P |
24 | rs104894551 CM023602 | dbSNP SNPDBe OMIM HGMD | Multiple independent submissions to the refSNP cluster by cluster Zeng (2002) J Inherit Metab Dis 25 | missense | E24G |
26 | rs145616193 | dbSNP | synonymous | T26T | |
27 | CM960085 | SNPDBe HGMD | Kaul (1996) Am J Hum Genet 59 | missense | G27R |
33 | rs138158568 | dbSNP SNPDBe | missense | H33R | |
53 | rs17850703 | dbSNP SNPDBe | missense | T53A | |
57 | CM001609 | SNPDBe HGMD | Sistermans (2000) Eur J Hum Genet 8 | missense | A57T |
68 | CM023603 | SNPDBe HGMD | Zeng (2002) J Inherit Metab Dis 25 | missense | D68A |
71 | rs104894553 CM060201 | dbSNP SNPDBe HGMD | multiple independent submissions to the refSNP cluster by cluster Janson (2006) Ann Neurol 59 | missense | R71H |
71_2 | SNPDBe | missense | R71K | ||
82 | rs80099330 | dbSNP SNPDBe | Multiple independent submissions to the refSNP cluster Validated by frequency or genotype data 1000Genome project 1000Genomes frequency cluster | missense | M82T |
93 | rs144639820 | dbSNP | Validated by frequency or genotype data | synonymous | A93A |
109 | CM990192 | HGMD | Elpeleg (1999) J Inherit Metab Dis 22 | nonsense | Y109Ter |
111 | rs181347986 | dbSNP SNPDBe | 1000Genome project 1000Genomes | missense | I111V |
114 | CM023014 | SNPDBe HGMD | Olsen (2002) J Med Genet 39 | missense | D114Y |
114_2 | CM960086 | HGMD | Kaul (1996) Am J Hum Genet 59 | missense | D114E |
121 | rs148451498 | dbSNP SNPDBe | missense | N121D | |
121_2 | CM063846 | HGMD | Zeng (2006) Mol Genet Metab 89 | missense | N121I |
123 | CM960087 | SNPDBe HGMD | Kaul (1996) Am J Hum Genet 59 | missense | G123E |
143_2 | CM063849 | HGMD | Zeng (2006) Mol Genet Metab 89 | missense | I143F |
143 | rs199565861 | dbSNP SNPDBe | 1000Genomes | missense | I143V |
152 | rs104894548 CM950102 | dbSNP SNPDBe OMIM HGMD | Multiple independent submissions to the refSNP cluster by cluster Kaul (1995) Hum Mutat 5 | missense | C152R |
152_2 | CM023604 | HGMD | Zeng (2002) J Inherit Metab Dis 25 | missense | C152W |
153 | rs141755746 | dbSNP | synonymous | Y153Y | |
154 | rs147193431 rs2228435 | dbSNP SNPDBe | missense | V154I | |
157 | rs140357187 | dbSNP SNPDBe | missense | I157T | |
164 | SNPDBe | missense | Y164F | ||
166 | CM063847 | HGMD | Zeng (2006) Mol Genet Metab 89 | missense | T166I |
168 | CM001610 | SNPDBe HGMD | Sistermans (2000) Eur J Hum Genet 8 | missense | R168H |
168_2 | CM960089 | HGMD | Kaul (1996) Am J Hum Genet 59 | missense | R168C |
170 | rs144321760 | dbSNP SNPDBe | Validated by frequency or genotype data by freq | missense | I170T |
178 | SNPDBe | missense | E178A | ||
181_2 | CM063850 | HGMD | Zeng (2006) Mol Genet Metab 89 | missense | P181L |
181 | CM001611 | SNPDBe HGMD | Sistermans (2000) Eur J Hum Genet 8 | missense | P181T |
183 | CM990193 | SNPDBe HGMD | Elpeleg (1999) J Inherit Metab Dis 22 | missense | P183H |
184 | CM023605 | HGMD | Zeng (2002) J Inherit Metab Dis 25 | nonsense | Q184Ter |
186 | CM990194 | SNPDBe HGMD | Elpeleg (1999) J Inherit Metab Dis 22 | missense | V186F |
195 | CM990195 | SNPDBe HGMD | Elpeleg (1999) J Inherit Metab Dis 22 | missense | M195R |
202 | rs147763700 | dbSNP SNPDBe | missense | A202S | |
213 | CM055097 | HGMD | Tacke (2005) Neuropediatrics 36 | missense | K213E |
214 | CM023606 | HGMD | Zeng (2002) J Inherit Metab Dis 25 | nonsense | E214Ter |
218 | rs104894549 | dbSNP | Multiple independent submissions to the refSNP cluster | nonsense | C218X |
218_2 | CM950103 | HGMD | Shaag (1995) Am J Hum Genet 57 | nonsense | C218Ter |
220 | rs139053885 | dbSNP SNPDBe | missense | I220T | |
226_2 | CM086530 | HGMD | Di Pietro (2008) Clin Biochem 41 | missense | I226T |
226 | rs201887670 | dbSNP | missense | I226K | |
231 | rs104894550 CM994594 | dbSNP SNPDBe OMIM HGMD | Multiple independent submissions to the refSNP cluster by cluster Rady (1999) Am J Med Genet 87 | missense | Y231C |
231_2 | CM940123 | HGMD | Kaul (1994) Am J Hum Genet 55 | nonsense | Y231Ter |
235 | rs149842031 | dbSNP SNPDBe | Multiple independent submissions to the refSNP cluster Validated by frequency or genotype data 1000Genome project 1000Genomes frequency cluster | missense | E235K |
236 | rs149189911 | dbSNP | synonymous | N236N | |
239 | rs145085349 | dbSNP SNPDBe | missense | I239T | |
244 | CM023607 | SNPDBe HGMD | Zeng (2002) J Inherit Metab Dis 25 | missense | H244R |
244_2 | CM063848 | HGMD | Zeng (2006) Mol Genet Metab 89 | missense | H244L |
249 | rs104894552 CM023015 | dbSNP SNPDBe HGMD | Multiple independent submissions to the refSNP cluster by cluster Olsen (2002) J Med Genet 39 | missense | D249V |
270 | rs200126822 | dbSNP SNPDBe | 1000Genomes | missense | I270T |
272 | CM063851 | HGMD | Zeng (2006) Mol Genet Metab 89 | missense | L272P |
274 | CM950104 | SNPDBe HGMD | Shaag (1995) Am J Hum Genet 57 | missense | G274R |
277 | rs78677072 | dbSNP | Multiple independent submissions to the refSNP cluster 1000Genome project | synonymous | T277T |
278 | rs140581464 | dbSNP SNPDBe | Multiple independent submissions to the refSNP cluster Validated by frequency or genotype data 1000Genome project 1000Genomes frequency cluster | missense | V278M |
279 | rs145717248 | dbSNP SNPDBe | missense | Y279H | |
280 | rs148081446 | dbSNP | Multiple independent submissions to the refSNP cluster Validated by frequency or genotype data 1000Genome project | synonymous | P280P |
280_2 | CM990197 | HGMD | Elpeleg (1999) J Inherit Metab Dis 22 | missense | P280S |
281 | rs141858640 | dbSNP SNPDBe | missense | V281M | |
285 | rs28940279 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 | missense | E285A |
285_2 | SNPDBe | missense | E285D | ||
286 | rs138062143 | dbSNP | synonymous | A286A | |
287 | CM990198 | SNPDBe HGMD | Elpeleg (1999) J Inherit Metab Dis 22 | missense | A287T |
288 | SNPDBe | missense | Y288F | ||
288_2 | CM034717 | HGMD | Surendran (2003) Mol Genet Metab 80 | missense | Y288C |
295 | CM950105 | SNPDBe HGMD | Shaag (1995) Am J Hum Genet 57 | missense | F295S |
305 | rs28940574 CM940124 | dbSNP SNPDBe OMIM HGMD | Multiple independent submissions to the refSNP cluster by cluster Kaul (1994) Am J Hum Genet 55 | missense | A305E |
310 | SNPDBe | missense | C310G | ||
314 | CM023608 | HGMD | Zeng (2002) J Inherit Metab Dis 25 | missense | Ter314W |
MTSCHIAEEHIQKVAIFGGTHGNELTGVFLVKHWLENGAEIQRTGLEVKPFITNPRAVKKCTRYIDCDLNRIFDLENLGKKMSEDLPYEVRRAQEINHLF R G T R P G TR R A T A K T A GPKDSEDSYDIIFDLHNTTSNMGCTLILEDSRNNFLIQMFHYIKTSLAPLPCYVYLIEHPSLKYATTRSIAKYPVGIEVGPQPQGVLRADILDQMRKMIK r V Y D E V RYI T F I H T A T Hr F R HALDFIHHFNEGKEFPPCAIEVYKIIEKVDYPRDENGEIAAIIHPNLQDQDWKPLHPGDPMFLTLDGKTIPLGGDCTVYPVFVNEAAYYEKKEAFAKTTK S Er r T K r KN T R V T P R TMHLM AATF S LTLNAKSIRCCLH- E G W