Product Details

SNP ID

rs200971843

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:38086442 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCGAGGCTGTGGCTGCCCCGGAGTG[G/T]GTAGGACCTAAGTCCAGAGAAAGGA

Phenotype

MIM: 610409

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

BAIAP2L2 PubMed Links

Gene Details

Gene

BAIAP2L2

Gene Name

BAI1 associated protein 2 like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025045.5	1693	Missense Mutation	ACA,CCA	T423P	NP_079321.3
XM_005261751.4	1693	Missense Mutation	ACA,CCA	T423P	XP_005261808.1
XM_011530379.2	1693	Missense Mutation	ACA,CCA	T423P	XP_011528681.1
XM_011530380.2	1693	Missense Mutation	ACA,CCA	T405P	XP_011528682.1
XM_011530381.2	1693	Missense Mutation	ACA,CCA	T404P	XP_011528683.1
XM_011530382.2	1693	Missense Mutation	ACA,CCA	T404P	XP_011528684.1
XM_011530383.2	1693	Missense Mutation	ACA,CCA	T399P	XP_011528685.1
XM_011530384.2	1693	Missense Mutation	ACA,CCA	T393P	XP_011528686.1
XM_011530386.2	1693	Missense Mutation	ACA,CCA	T228P	XP_011528688.1
XM_011530387.2	1693	Missense Mutation	ACA,CCA	T228P	XP_011528689.1
XM_011530388.2	1693	Missense Mutation	ACA,CCA	T216P	XP_011528690.1

Gene

SLC16A8

Gene Name

solute carrier family 16 member 8

There are no transcripts associated with this gene.

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