Product Details

SNP ID

rs5964989

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:65607173 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CATTTCTAAGAGAGAGAAATTGAGG[C/T]GAGAGAAGTTTAGCAACTTGCCTTA

Phenotype

MIM: 309845

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MSN PubMed Links

Gene Details

Gene

MSN

Gene Name

moesin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002444.2		Intron			NP_002435.1
XM_005262269.2		Intron			XP_005262326.1
XM_011530959.1		Intron			XP_011529261.1
XM_017029545.1		Intron			XP_016885034.1
XM_017029546.1		Intron			XP_016885035.1

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