Product Details

SNP ID
rs149942472
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.20:1443758 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGCTGGCTGGGCGGTTATGTTAA[C/G]CGCTGCACGATGACAGCATTGAGCA
Phenotype
MIM: 606610
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
NSFL1C PubMed Links

Gene Details

Gene
NSFL1C
Gene Name
NSFL1 cofactor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206736.1 2529 Silent Mutation CGC,CGG R370R NP_001193665.1
NM_016143.4 2529 Silent Mutation CGC,CGG R368R NP_057227.2
NM_018839.4 2529 Silent Mutation CGC,CGG R337R NP_061327.2
XM_006723592.2 2529 Silent Mutation CGC,CGG R259R XP_006723655.1
XM_006723593.2 2529 Silent Mutation CGC,CGG R259R XP_006723656.1
XM_006723594.2 2529 Silent Mutation CGC,CGG R257R XP_006723657.1
XM_011529300.1 2529 Silent Mutation CGC,CGG R373R XP_011527602.1
XM_011529301.1 2529 Silent Mutation CGC,CGG R371R XP_011527603.1
XM_011529302.2 2529 Silent Mutation CGC,CGG R320R XP_011527604.1
XM_011529304.1 2529 Silent Mutation CGC,CGG R317R XP_011527606.1
XM_011529305.2 2529 Intron XP_011527607.1
XM_017027956.1 2529 Silent Mutation CGC,CGG R318R XP_016883445.1
XM_017027957.1 2529 Silent Mutation CGC,CGG R319R XP_016883446.1
XM_017027958.1 2529 Silent Mutation CGC,CGG R283R XP_016883447.1

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