Product Details

SNP ID

rs145071913

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:12661334 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGGAAGGGATTTCTGAAATGCCA[A/G]CGTAGTTTTTTTTGGCCATCCTTGA

Phenotype

MIM: 602927

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

GPR19 PubMed Links

Gene Details

Gene

GPR19

Gene Name

G protein-coupled receptor 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006143.2	3813	Missense Mutation	GCT,GTT	A372V	NP_006134.1
XM_011520623.2	3813	Missense Mutation	GCT,GTT	A391V	XP_011518925.1
XM_011520624.2	3813	Missense Mutation	GCT,GTT	A391V	XP_011518926.1
XM_011520625.2	3813	Missense Mutation	GCT,GTT	A372V	XP_011518927.1
XM_017019212.1	3813	Missense Mutation	GCT,GTT	A391V	XP_016874701.1
XM_017019213.1	3813	Missense Mutation	GCT,GTT	A391V	XP_016874702.1
XM_017019214.1	3813	Missense Mutation	GCT,GTT	A391V	XP_016874703.1
XM_017019215.1	3813	Missense Mutation	GCT,GTT	A391V	XP_016874704.1
XM_017019216.1	3813	Missense Mutation	GCT,GTT	A372V	XP_016874705.1

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