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QuickView for rs115944950;jsessionid=1E271BCFCC6CA21497D1FE168F144B52 (snp)

Summary
General Info

- Macaque -
- - Human G|C
  - Chimp -
- Mouse -
- Rat -

Type:: SNP
Organism:: Homo sapiens
Alleles:: G|C
Chromosomal Location:: chr 2 : 234345731 (build 36.3)
Strand:: +
Update Date:: Nov 14 2011
Associated Gene(s):: UGT1A4, UGT1A10, UGT1A1, UGT1A5, UGT1A9, more ...
Related URLs:: NCBI dbSNP

UGT1A4 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_007120	G1392C	NP_009051	Missense	E464D

UGT1A10 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_019075	G1380C	NP_061948	Missense	E460D

UGT1A1 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_000463	G1389C	NP_000454	Missense	E463D

UGT1A5 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_019078	G1392C	NP_061951	Missense	E464D

UGT1A9 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_021027	G1380C	NP_066307	Missense	E460D

UGT1A8 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_019076	G1380C	NP_061949	Missense	E460D

UGT1A3 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_019093	G1392C	NP_061966	Missense	E464D

UGT1A7 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_019077	G1380C	NP_061950	Missense	E460D

UGT1A6 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_001072	G1386C	NP_001063	Missense	E462D
NM_205862	G585C	NP_995584	Missense	E195D