Product Details

SNP ID
rs1065310
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:151405165 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GATTACAGGCATGAGGCACCGCGCC[C/G]GGCCGAACATTTAATTTTTGATTGT
Phenotype
MIM: 614917
Polymorphism
C/G, Transversion 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 1600 UTR 3 NP_001258866.1
NM_017909.3 1600 UTR 3 NP_060379.2
XM_005267040.3 1600 UTR 3 XP_005267097.1
XM_017010988.1 1600 UTR 3 XP_016866477.1

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