Product Details

SNP ID
rs200224785
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:47618860 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAATTAACATTTTCAGGTCACAACA[A/G]TAAGTCTTCCCAAAGGGGACCTTCC
Phenotype
MIM: 613221
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MTCH2 PubMed Links

Gene Details

Gene
MTCH2
Gene Name
mitochondrial carrier 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001317231.1 969 Silent Mutation TAC,TAT Y295Y NP_001304160.1
NM_001317232.1 969 Silent Mutation TAC,TAT Y286Y NP_001304161.1
NM_001317233.1 969 Silent Mutation TAC,TAT Y147Y NP_001304162.1
NM_014342.3 969 Silent Mutation TAC,TAT Y295Y NP_055157.1
XM_006718172.2 969 UTR 3 XP_006718235.1
XM_011519959.2 969 Intron XP_011518261.1
XM_011519960.2 969 Intron XP_011518262.1
XM_011519961.2 969 Intron XP_011518263.1
XM_017017462.1 969 UTR 3 XP_016872951.1
XM_017017463.1 969 Silent Mutation TAC,TAT Y168Y XP_016872952.1

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