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SNP ID: rs236189
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:5951544 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GATTTACAGAAAAACTGCACAAAAA[A/G]TGGATGTGACACTGCAGGATTGACT
Phenotype: MIM: 608187
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: MCM8 PubMed Links

Gene Details

Gene: MCM8
Gene Name: minichromosome maintenance 8 homologous recombination repair factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001281520.1		Intron			NP_001268449.1
NM_001281521.1		Intron			NP_001268450.1
NM_001281522.1		Intron			NP_001268451.1
NM_032485.5		Intron			NP_115874.3
NM_182802.2		Intron			NP_877954.1
XM_011529387.2		Intron			XP_011527689.1
XM_017028105.1		Intron			XP_016883594.1
XM_017028106.1		Intron			XP_016883595.1
XM_017028107.1		Intron			XP_016883596.1

Gene: TRMT6
Gene Name: tRNA methyltransferase 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001281467.1		Intron			NP_001268396.1
NM_015939.4		Intron			NP_057023.2
XM_017027875.1		Intron			XP_016883364.1

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