Product Details

SNP ID: rs140869795
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:1584579 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGACCCGCAGCCTCCCTTAGACCCC[A/G]CGCAAGAGCCACAACTGGAACAGGA
Phenotype: MIM: 148022
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: KRTAP5-1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001005922.1	705	Missense Mutation			NP_001005922.1

There are no transcripts associated with this gene.