Product Details

SNP ID

rs143349898

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:36952886 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTTCTTCCCTCTCTTCTTTGTAG[A/G]TGAGGAAATATCTGATGAGGAAGGG

Phenotype

MIM: 608463 MIM: 601999

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

AATF PubMed Links

Gene Details

Gene

AATF

Gene Name

apoptosis antagonizing transcription factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012138.3	535	Missense Mutation	GAT,GGT	D95G	NP_036270.1
XM_011524611.1	535	Missense Mutation	GAT,GGT	D95G	XP_011522913.1

Gene

LHX1

Gene Name

LIM homeobox 1

There are no transcripts associated with this gene.

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