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SNP ID

rs201698250

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:86751916 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCAGAATTTTGATTCTGACATTAG[C/T]AGTGTGGGAATAGATGGCTGCTGGC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RMND5A PubMed Links

Gene Details

Gene

RMND5A

Gene Name

required for meiotic nuclear division 5 homolog A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022780.3	683	Silent Mutation	AGC,AGT	S102S	NP_073617.1

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