Product Details

SNP ID

rs17022762

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:99551796 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTATATCCAAATAAATAAATACA[A/T]GATATCTGCCATTTCTAACTCAAAT

Phenotype

MIM: 601464

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

AFF3 PubMed Links

Gene Details

Gene

AFF3

Gene Name

AF4/FMR2 family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001025108.1		Intron			NP_001020279.1
NM_002285.2		Intron			NP_002276.2
XM_005263943.3		Intron			XP_005264000.2
XM_005263945.3		Intron			XP_005264002.1
XM_011511169.2		Intron			XP_011509471.1
XM_011511170.2		Intron			XP_011509472.1
XM_011511171.2		Intron			XP_011509473.1
XM_011511172.2		Intron			XP_011509474.1
XM_011511173.2		Intron			XP_011509475.1
XM_011511174.2		Intron			XP_011509476.1
XM_011511175.2		Intron			XP_011509477.1
XM_011511176.2		Intron			XP_011509478.1
XM_011511177.2		Intron			XP_011509479.1
XM_011511178.2		Intron			XP_011509480.1
XM_011511179.2		Intron			XP_011509481.1
XM_017004085.1		Intron			XP_016859574.1
XM_017004086.1		Intron			XP_016859575.1
XM_017004087.1		Intron			XP_016859576.1

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