Product Details

SNP ID
rs79431092
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:78922364 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTTATTTGATCACCGGCAAATCA[C/T]GGACCTGACTTTGTGAAGAATTCAT
Phenotype
MIM: 116820
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CTSH PubMed Links

Gene Details

Gene
CTSH
Gene Name
cathepsin H
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001319137.1 Intron NP_001306066.1
NM_004390.4 Intron NP_004381.2
XM_005254181.2 Intron XP_005254238.1
XM_011521276.1 Intron XP_011519578.1
XM_017021951.1 Intron XP_016877440.1
XM_017021952.1 Intron XP_016877441.1

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