Product Details

SNP ID
rs151046793
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:63970065 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATCGAACGGTTCTGAGTCATCTGC[C/T]GGAAGCCTTGCCCTCAATCAAGGCG
Phenotype
MIM: 612086 MIM: 601697
Polymorphism
C/T, 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 37 Intron NP_001116838.1
XM_011525930.2 37 Intron XP_011524232.1
XM_017025710.1 37 Intron XP_016881199.1
Gene
SERPINB8
Gene Name
serpin family B member 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001031848.1 37 UTR 5 NP_001027018.1
NM_001276490.1 37 UTR 5 NP_001263419.1
NM_002640.3 37 UTR 5 NP_002631.3
NM_198833.1 37 UTR 5 NP_942130.1
XM_006722484.2 37 Intron XP_006722547.1
XM_011526025.1 37 UTR 5 XP_011524327.1
XM_017025790.1 37 UTR 5 XP_016881279.1
XM_017025791.1 37 Intron XP_016881280.1
XM_017025792.1 37 Intron XP_016881281.1

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