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SNP ID

rs150401054

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:37695029 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGATCCAGGCTTGGGAGTTGTGG[G/T]ACATCACTTCTGCTTCCTTCTCATT

Phenotype

MIM: 314850

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

XK PubMed Links

Gene Details

Gene

XK

Gene Name

X-linked Kx blood group

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011543978.2		Intron			XP_011542280.1

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