Product Details

SNP ID

rs12670233

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.7:32505978 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CAAAGATTCTAAGTCCGTAAAGTGT[A/G]CCCTAAACATAATCTCTGCTTGTTA

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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