Product Details

SNP ID
rs146761360
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:197791401 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTCCGGGGCAGGCCCTGGTTTTGG[C/T]CCGGGCTCGTGGAGCCGCTCTCTCG
Phenotype
MIM: 616933
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FYTTD1 PubMed Links

Gene Details

Gene
FYTTD1
Gene Name
forty-two-three domain containing 1
There are no transcripts associated with this gene.

Gene
LRCH3
Gene Name
leucine rich repeats and calponin homology domain containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032773.3 176 Silent Mutation GGC,GGT G41G NP_116162.1
XM_005269362.2 176 Silent Mutation GGC,GGT G41G XP_005269419.1
XM_005269363.2 176 Silent Mutation GGC,GGT G41G XP_005269420.1
XM_005269365.2 176 Silent Mutation GGC,GGT G41G XP_005269422.1
XM_005269367.2 176 Silent Mutation GGC,GGT G41G XP_005269424.1
XM_006713791.3 176 Silent Mutation GGC,GGT G41G XP_006713854.1
XM_006713792.3 176 Silent Mutation GGC,GGT G41G XP_006713855.1
XM_006713793.2 176 Silent Mutation GGC,GGT G41G XP_006713856.1
XM_011513242.2 176 Silent Mutation GGC,GGT G41G XP_011511544.1
XM_011513243.2 176 Silent Mutation GGC,GGT G41G XP_011511545.1
XM_017007350.1 176 Silent Mutation GGC,GGT G41G XP_016862839.1
XM_017007351.1 176 Silent Mutation GGC,GGT G41G XP_016862840.1
XM_017007352.1 176 Silent Mutation GGC,GGT G41G XP_016862841.1

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