Product Details

SNP ID

rs13208602

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:151410814 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TATTTGCAGTATAACGAAAGATAAC[C/T]GTTTTTATACATTGATCTTGAGACC

Phenotype

MIM: 614917

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RMND1 PubMed Links

Gene Details

Gene

RMND1

Gene Name

required for meiotic nuclear division 1 homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271937.1		Intron			NP_001258866.1
NM_017909.3		Intron			NP_060379.2
XM_005267040.3		Intron			XP_005267097.1
XM_017010988.1		Intron			XP_016866477.1

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