Product Details

SNP ID

rs10268803

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:32508223 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTACACCATAATTGAAATGTGGTCA[A/G]CTATATTAGTCTTTCCCATTGTGGT

Phenotype

MIM: 612927

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

AVL9 PubMed Links

Gene Details

Gene

AVL9

Gene Name

AVL9 cell migration associated

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015060.2		Intron			NP_055875.1
XM_005249668.2		Intron			XP_005249725.1
XM_005249669.2		Intron			XP_005249726.1
XM_005249670.2		Intron			XP_005249727.1
XM_005249671.4		Intron			XP_005249728.1
XM_011515227.2		Intron			XP_011513529.1
XM_017011891.1		Intron			XP_016867380.1
XM_017011892.1		Intron			XP_016867381.1

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