Product Details

SNP ID
rs75322378
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:49416018 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATAGCCTGCAGCCTCATCATTTCC[C/T]ATCTGGACCTGGTACAAATGCACGT
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
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000481.3 1689 Intron NP_000472.2
NM_001164710.1 1689 Intron NP_001158182.1
NM_001164711.1 1689 Intron NP_001158183.1
NM_001164712.1 1689 Intron NP_001158184.1
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 1689 UTR 3 NP_071503.1

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