Product Details

SNP ID
rs140995041
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:49414851 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCAGCAAACGAACCTCTCAAAACC[C/T]ACAGAGAATAAGGGAAGGCAGCAGA
Phenotype
MIM: 238310 MIM: 611516 MIM: 165390 MIM: 600690
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
AMT PubMed Links

Gene Details

Gene
AMT
Gene Name
aminomethyltransferase
There are no transcripts associated with this gene.

Gene
NICN1
Gene Name
nicolin 1
There are no transcripts associated with this gene.

Gene
RHOA
Gene Name
ras homolog family member A
There are no transcripts associated with this gene.

Gene
TCTA
Gene Name
T-cell leukemia translocation altered
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022171.2 522 Missense Mutation CAC,TAC H101Y NP_071503.1

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