Product Details

SNP ID

rs10807861

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:32585342 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGACATCTGTCATCTGAGAAAGGA[C/T]ATCTGGTTTCATGTTAGGCACATAC

Phenotype

MIM: 612927

Polymorphism

C/T, 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	3443	UTR 3			NP_055875.1
XM_005249668.2	3443	UTR 3			XP_005249725.1
XM_005249669.2	3443	UTR 3			XP_005249726.1
XM_005249670.2	3443	UTR 3			XP_005249727.1
XM_005249671.4	3443	Intron			XP_005249728.1
XM_011515227.2	3443	UTR 3			XP_011513529.1
XM_017011891.1	3443	UTR 3			XP_016867380.1
XM_017011892.1	3443	UTR 3			XP_016867381.1

Gene

DPY19L1P1

Gene Name

DPY19L1 pseudogene 1

There are no transcripts associated with this gene.

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