Product Details

SNP ID

rs16868116

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:39111501 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAAACATGAAAATATTTTTTAAAAG[G/T]TGGAATCATAAAACTGAATTTATAC

Phenotype

MIM: 602731

Polymorphism

G/T, Transversion 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		Intron			NP_001230022.1
NM_001465.4		Intron			NP_001456.3
NM_199335.3		Intron			NP_955367.1
XM_006714464.2		Intron			XP_006714527.1
XM_006714465.2		Intron			XP_006714528.1
XM_006714466.2		Intron			XP_006714529.1
XM_011514008.2		Intron			XP_011512310.1
XM_011514009.1		Intron			XP_011512311.1
XM_011514010.1		Intron			XP_011512312.1
XM_011514011.2		Intron			XP_011512313.1
XM_011514012.2		Intron			XP_011512314.1
XM_011514013.2		Intron			XP_011512315.1
XM_017009316.1		Intron			XP_016864805.1

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