Product Details

SNP ID
rs61738713
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:63954539 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGCCAACGGGCTCTTTGGAGAAAA[A/G]TCTTATGATTTCCTCACAGTAAGTC
Phenotype
MIM: 612086
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HMSD PubMed Links

Gene Details

Gene
HMSD
Gene Name
histocompatibility minor serpin domain containing
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001123366.1 448 Silent Mutation AAA,AAG K68K NP_001116838.1
XM_011525930.2 448 Silent Mutation AAA,AAG K68K XP_011524232.1
XM_017025710.1 448 Silent Mutation AAA,AAG K68K XP_016881199.1

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