Product Details

SNP ID

rs146479455

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:39107463 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGTGCTAGTCATTGTCATAGATGC[A/G]GCCTGAAAGGAAAAAATACAAATTT

Phenotype

MIM: 602731

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FYB PubMed Links

Gene Details

Gene

FYB

Gene Name

FYN binding protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243093.1	2456	Missense Mutation	CGC,TGC	R834C	NP_001230022.1
NM_001465.4	2456	Missense Mutation	CGC,TGC	R824C	NP_001456.3
NM_199335.3	2456	Missense Mutation	CGC,TGC	R778C	NP_955367.1
XM_006714464.2	2456	Missense Mutation	CGC,TGC	R824C	XP_006714527.1
XM_006714465.2	2456	Missense Mutation	CGC,TGC	R824C	XP_006714528.1
XM_006714466.2	2456	Missense Mutation	CGC,TGC	R824C	XP_006714529.1
XM_011514008.2	2456	Missense Mutation	CGC,TGC	R834C	XP_011512310.1
XM_011514009.1	2456	Missense Mutation	CGC,TGC	R824C	XP_011512311.1
XM_011514010.1	2456	Missense Mutation	CGC,TGC	R824C	XP_011512312.1
XM_011514011.2	2456	Missense Mutation	CGC,TGC	R788C	XP_011512313.1
XM_011514012.2	2456	Intron			XP_011512314.1
XM_011514013.2	2456	Intron			XP_011512315.1
XM_017009316.1	2456	Missense Mutation	CGC,TGC	R788C	XP_016864805.1

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