Product Details

SNP ID

rs686941

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:63970263 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTCCCTGGAGTGCGTGAGAGAGG[C/G]GAAGGGAGGAAGGCCAGAGCAGGAA

Phenotype

MIM: 612086 MIM: 601697

Polymorphism

C/G, Transversion 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		Intron			NP_001116838.1
XM_011525930.2		Intron			XP_011524232.1
XM_017025710.1		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		Intron			NP_001027018.1
NM_001276490.1		Intron			NP_001263419.1
NM_002640.3		Intron			NP_002631.3
NM_198833.1		Intron			NP_942130.1
XM_006722484.2		Intron			XP_006722547.1
XM_011526025.1		Intron			XP_011524327.1
XM_017025790.1		Intron			XP_016881279.1
XM_017025791.1		Intron			XP_016881280.1
XM_017025792.1		Intron			XP_016881281.1

View Full Product Details