Product Details

SNP ID

rs9960367

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:63952945 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTATTGGAAATCAATAGTTTTTCT[C/T]CTTACAAATTTCATGTTTTAAGCAA

Phenotype

MIM: 612086

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		Intron			NP_001116838.1
XM_011525930.2		Intron			XP_011524232.1
XM_017025710.1		Intron			XP_016881199.1

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