Product Details

SNP ID
rs114898155
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:131711310 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGAGGCCGGGCCAGGCGGTGCCGG[C/T]GGTGGGGGCAGCCGAGTGGAGCTCT
Phenotype
MIM: 601945
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SFSWAP PubMed Links

Gene Details

Gene
SFSWAP
Gene Name
splicing factor SWAP homolog
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001261411.1 223 Silent Mutation GGC,GGT G27G NP_001248340.1
NM_004592.3 223 Silent Mutation GGC,GGT G27G NP_004583.2
XM_011538653.1 223 Silent Mutation GGC,GGT G27G XP_011536955.1
XM_011538654.2 223 UTR 5 XP_011536956.1
XM_011538655.2 223 Silent Mutation GGC,GGT G27G XP_011536957.1
XM_017019798.1 223 Silent Mutation GGC,GGT G27G XP_016875287.1
XM_017019799.1 223 UTR 5 XP_016875288.1

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