Product Details

SNP ID

rs181956190

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:44662324 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTCTTAAAACTTTCAGAGTGAAG[A/G]CAATGTAGACCTAAGGCAGACCTAT

Phenotype

MIM: 616934

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MEIOC PubMed Links

Gene Details

Gene

MEIOC

Gene Name

meiosis specific with coiled-coil domain

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145080.2	409	Missense Mutation	GAC,GGC	D71G	NP_001138552.2
XM_005257236.3	409	Missense Mutation	GAC,GGC	D71G	XP_005257293.1

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