Product Details

SNP ID
rs144434177
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:113299863 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGTAGAAGAGGAGCAGGCAGAAGC[C/T]ATAGACTCTGCTGAGCTGGAAGCAC
Phenotype
MIM: 609841 MIM: 609666
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MIR6762 PubMed Links

Gene Details

Gene
MIR6762
Gene Name
microRNA 6762
There are no transcripts associated with this gene.

Gene
SLC8B1
Gene Name
solute carrier family 8 member B1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_006719607.2 2283 Missense Mutation AGC,GGC S362G XP_006719670.1
XM_011538749.2 2283 Missense Mutation AGC,GGC S557G XP_011537051.1
XM_011538750.2 2283 Missense Mutation AGC,GGC S501G XP_011537052.1
XM_011538752.2 2283 Missense Mutation AGC,GGC S362G XP_011537054.1
XM_017019978.1 2283 Intron XP_016875467.1
Gene
TPCN1
Gene Name
two pore segment channel 1
There are no transcripts associated with this gene.

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