Product Details

SNP ID: rs61742362
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:118814970 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAAGATTTCCTTTTACTGACACGCA[C/T]TGGAGCTGTGGTTGTAGGAGGGGAG
Phenotype: MIM: 610098
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: MCM9 PubMed Links

Gene Details

Gene: MCM9
Gene Name: minichromosome maintenance 9 homologous recombination repair factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017696.2	3301	Missense Mutation	ATG,GTG	M1096V	NP_060166.2
NM_153255.4	3301	Intron			NP_694987.1