Product Details

SNP ID

rs17794321

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:23346681 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGGGTTGGGGGTGGCAAGCAGCGG[A/G]ACGTGGTCACAGCGGGTAGGGGGTG

Phenotype

MIM: 609906 MIM: 611461

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

EFS PubMed Links

Gene Details

Gene

EFS

Gene Name

embryonal Fyn-associated substrate

There are no transcripts associated with this gene.

Gene

SLC22A17

Gene Name

solute carrier family 22 member 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001289050.1	2034	Silent Mutation	GTC,GTT	V292V	NP_001275979.1
NM_016609.4	2034	Silent Mutation	GTC,GTT	V510V	NP_057693.3
NM_020372.3	2034	Silent Mutation	GTC,GTT	V528V	NP_065105.2
XM_005267747.4	2034	Silent Mutation	GTC,GTT	V528V	XP_005267804.1
XM_005267748.4	2034	Silent Mutation	GTC,GTT	V402V	XP_005267805.1
XM_017021361.1	2034	Silent Mutation	GTC,GTT	V528V	XP_016876850.1
XM_017021362.1	2034	Silent Mutation	GTC,GTT	V510V	XP_016876851.1

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