Product Details

SNP ID
rs142930455
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:43432211 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACTTGCAGCTTCCTTCCTGCTTTC[C/T]GTCTTCCCGCTGCTAGACCTTCTTC
Phenotype
MIM: 612509
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ABCC10 PubMed Links

Gene Details

Gene
ABCC10
Gene Name
ATP binding cassette subfamily C member 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001198934.1 446 Silent Mutation TCC,TCT S77S NP_001185863.1
NM_033450.2 446 Silent Mutation TCC,TCT S34S NP_258261.2
XM_011514974.2 446 Silent Mutation TCC,TCT S128S XP_011513276.2
XM_011514983.2 446 Intron XP_011513285.1
XM_011514985.2 446 Intron XP_011513287.1
XM_011514986.2 446 Intron XP_011513288.1
XM_017011445.1 446 Silent Mutation TCC,TCT S128S XP_016866934.1
XM_017011446.1 446 Silent Mutation TCC,TCT S77S XP_016866935.1
XM_017011447.1 446 Silent Mutation TCC,TCT S77S XP_016866936.1
XM_017011448.1 446 Silent Mutation TCC,TCT S128S XP_016866937.1
XM_017011449.1 446 Silent Mutation TCC,TCT S128S XP_016866938.1
XM_017011450.1 446 Silent Mutation TCC,TCT S128S XP_016866939.1
XM_017011451.1 446 Silent Mutation TCC,TCT S128S XP_016866940.1
XM_017011452.1 446 UTR 5 XP_016866941.1
XM_017011453.1 446 Silent Mutation TCC,TCT S128S XP_016866942.1
XM_017011454.1 446 Intron XP_016866943.1
XM_017011455.1 446 Intron XP_016866944.1
XM_017011456.1 446 Intron XP_016866945.1
Gene
MIR6780B
Gene Name
microRNA 6780b
There are no transcripts associated with this gene.

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