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QuickView for rs114982090;jsessionid=84ADD494D817F647C78A109985A5704D (snp)

Summary
General Info

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

Type:: SNP
Organism:: Homo sapiens
Alleles:: T|C
Chromosomal Location:: chr 2 : 234345694 (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	C1355T	NP_009051	Missense	P452L

UGT1A10 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_019075	C1343T	NP_061948	Missense	P448L

UGT1A1 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_000463	C1352T	NP_000454	Missense	P451L

UGT1A5 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_019078	C1355T	NP_061951	Missense	P452L

UGT1A9 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_021027	C1343T	NP_066307	Missense	P448L

UGT1A8 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_019076	C1343T	NP_061949	Missense	P448L

UGT1A3 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_019093	C1355T	NP_061966	Missense	P452L

UGT1A7 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_019077	C1343T	NP_061950	Missense	P448L

UGT1A6 (exon)

Transcript	CDS Change	Protein	Mutation Class	AA Change
NM_001072	C1349T	NP_001063	Missense	P450L
NM_205862	C548T	NP_995584	Missense	P183L