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SNP ID: rs147761911
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:233693273 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TATGACCAAGAAGAGCTGAAGAACC[A/G]TTACCAATCATTTGGAAACAATCAC
Phenotype: MIM: 606435 MIM: 606431 MIM: 606432 MIM: 606433 MIM: 606434
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: UGT1A10 PubMed Links

Gene Details

Gene: UGT1A10
Gene Name: UDP glucuronosyltransferase family 1 member A10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019075.2	408	Intron			NP_061948.1

Gene: UGT1A6
Gene Name: UDP glucuronosyltransferase family 1 member A6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001072.3	408	Missense Mutation	CAT,CGT	H90R	NP_001063.2
NM_205862.1	408	Intron			NP_995584.1

Gene: UGT1A7
Gene Name: UDP glucuronosyltransferase family 1 member A7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019077.2	408	Intron			NP_061950.2

Gene: UGT1A8
Gene Name: UDP glucuronosyltransferase family 1 member A8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019076.4	408	Intron			NP_061949.3

Gene: UGT1A9
Gene Name: UDP glucuronosyltransferase family 1 member A9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021027.2	408	Intron			NP_066307.1

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