Task 5 - Mapping SNPs Canavan

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 Position	Identifier	Reference DB	Year	SNP Type	Mutation
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
111	rs181347986	dbSNP SNPDBe	1000Genome project	missense	I111V
195	CM990195	SNPDBe HGMD	"Elpeleg (1999) J Inherit Metab Dis 22	missense	M195R
281	rs141858640	dbSNP SNPDBe		missense	V281M
280	rs148081446	dbSNP	Multiple independent submissions to the refSNP cluster Validated by frequency or genotype data 1000Genome project	synonymous	P280P
33	rs138158568	dbSNP SNPDBe		missense	H33R
157	rs140357187	dbSNP SNPDBe		missense	I157T
285	rs28940279 CM930046	dbSNP SNPDBe OMIM HGMD	Multiple independent submissions to the refSNP cluster Validated by frequency or genotype data "Kaul (1993) Nat Genet 5	missense	E285A
143_2	CM063849	HGMD	"Zeng (2006) Mol Genet Metab 89	missense	I143F
154	rs147193431 rs2228435	dbSNP SNPDBe		missense	V154I
288		SNPDBe		missense	Y288F
152	rs104894548 CM950102	dbSNP SNPDBe OMIM HGMD	Multiple independent submissions to the refSNP cluster "Kaul (1995) Hum Mutat 5	missense	C152R
153	rs141755746	dbSNP		synonymous	Y153Y
286	rs138062143	dbSNP		synonymous	A286A
287	CM990198	SNPDBe HGMD	"Elpeleg (1999) J Inherit Metab Dis 22	missense	A287T
82	rs80099330	dbSNP SNPDBe	Multiple independent submissions to the refSNP cluster Validated by frequency or genotype data 1000Genome project	missense	M82T
244	CM023607	SNPDBe HGMD	"Zeng (2002) J Inherit Metab Dis 25	missense	H244R
152_2	CM023604	HGMD	"Zeng (2002) J Inherit Metab Dis 25	missense	C152W
181_2	CM063850	HGMD	"Zeng (2006) Mol Genet Metab 89	missense	P181L
249	rs104894552 CM023015	dbSNP SNPDBe HGMD	Multiple independent submissions to the refSNP cluster "Olsen (2002) J Med Genet 39	missense	D249V
202	rs147763700	dbSNP SNPDBe		missense	A202S
68	CM023603	SNPDBe HGMD	"Zeng (2002) J Inherit Metab Dis 25	missense	D68A
121	rs148451498	dbSNP SNPDBe		missense	N121D
123	CM960087	SNPDBe HGMD	"Kaul (1996) Am J Hum Genet 59	missense	G123E
288_2	CM034717	HGMD	"Surendran (2003) Mol Genet Metab 80	missense	Y288C
305	rs28940574 CM940124	dbSNP SNPDBe OMIM HGMD	Multiple independent submissions to the refSNP cluster "Kaul (1994) Am J Hum Genet 55	missense	A305E
24	rs104894551 CM023602	dbSNP SNPDBe OMIM HGMD	Multiple independent submissions to the refSNP cluster "Zeng (2002) J Inherit Metab Dis 25	missense	E24G
270	rs200126822	dbSNP SNPDBe		missense	I270T
272	CM063851	HGMD	"Zeng (2006) Mol Genet Metab 89	missense	L272P
166	CM063847	HGMD	"Zeng (2006) Mol Genet Metab 89	missense	T166I
26	rs145616193	dbSNP		synonymous	T26T
27	CM960085	SNPDBe HGMD	"Kaul (1996) Am J Hum Genet 59	missense	G27R
274	CM950104	SNPDBe HGMD	"Shaag (1995) Am J Hum Genet 57	missense	G274R
168	CM001610	SNPDBe HGMD	"Sistermans (2000) Eur J Hum Genet 8	missense	R168H
239	rs145085349	dbSNP SNPDBe		missense	I239T
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	missense	V278M
164		SNPDBe		missense	Y164F
279	rs145717248	dbSNP SNPDBe		missense	Y279H
4	rs142041344	dbSNP SNPDBe		missense	C4R
231	rs104894550 CM994594	dbSNP SNPDBe OMIM HGMD	Multiple independent submissions to the refSNP cluster "Rady (1999) Am J Med Genet 87	missense	Y231C
71	rs104894553 CM060201	dbSNP SNPDBe HGMD	multiple independent submissions to the refSNP cluster "Janson (2006) Ann Neurol 59	missense	R71H
236	rs149189911	dbSNP		synonymous	N236N
235	rs149842031	dbSNP SNPDBe	Multiple independent submissions to the refSNP cluster Validated by frequency or genotype data 1000Genome project	missense	E235K
71_2		SNPDBe		missense	R71K
57	CM001609	SNPDBe HGMD	"Sistermans (2000) Eur J Hum Genet 8	missense	A57T
213	CM055097	HGMD	"Tacke (2005) Neuropediatrics 36	missense	K213E
214	CM023606	HGMD	"Zeng (2002) J Inherit Metab Dis 25	missense	E214Ter
314	CM023608	HGMD	"Zeng (2002) J Inherit Metab Dis 25	missense	Ter314W
18	CM067343	HGMD	"Zeng (2006) Adv Exp Med Biol 576	missense	G18R
178		SNPDBe		missense	E178A
218	rs104894549	dbSNP	Multiple independent submissions to the refSNP cluster	nonsense	C218X
16	CM960084	SNPDBe HGMD	"Kaul (1996) Am J Hum Genet 59	missense	I16T
310		SNPDBe		missense	C310G
14	CM063852	HGMD	"Zeng (2006) Mol Genet Metab 89	missense	V14G
170	rs144321760	dbSNP SNPDBe	Validated by frequency or genotype data	missense	I170T
21	CM001608	SNPDBe HGMD	"Sistermans (2000) Eur J Hum Genet 8	missense	H21P
226_2	CM086530	HGMD	"Di Pietro (2008) Clin Biochem 41	missense	I226T
109	CM990192	HGMD	"Elpeleg (1999) J Inherit Metab Dis 22	missense	Y109Ter
218_2	CM950103	HGMD	"Shaag (1995) Am J Hum Genet 57	missense	C218Ter
244_2	CM063848	HGMD	"Zeng (2006) Mol Genet Metab 89	missense	H244L
220	rs139053885	dbSNP SNPDBe		missense	I220T
143	rs199565861	dbSNP SNPDBe		missense	I143V
93	rs144639820	dbSNP	Validated by frequency or genotype data	synonymous	A93A
226	rs201887670	dbSNP		missense	I226K
121_2	CM063846	HGMD	"Zeng (2006) Mol Genet Metab 89	missense	N121I
231_2	CM940123	HGMD	"Kaul (1994) Am J Hum Genet 55	missense	Y231Ter
295	CM950105	SNPDBe HGMD	"Shaag (1995) Am J Hum Genet 57	missense	F295S
168_2	CM960089	HGMD	"Kaul (1996) Am J Hum Genet 59	missense	R168C
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	missense	Q184Ter
280_2	CM990197	HGMD	"Elpeleg (1999) J Inherit Metab Dis 22	missense	P280S
285_2		SNPDBe		missense	E285D
186	CM990194	SNPDBe HGMD	"Elpeleg (1999) J Inherit Metab Dis 22	missense	V186F
53	rs17850703	dbSNP SNPDBe		missense	T53A

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