Product Details

SNP ID: rs16934253
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:113299420 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGGGAACGGGCAGTGCCTGTGCCTC[A/G]GGGGTACCTCCAGCATGGCCTGGAG
Phenotype: MIM: 609841 MIM: 609666
Polymorphism: A/G, 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	2726	UTR 3			XP_006719670.1
XM_011538749.2	2726	UTR 3			XP_011537051.1
XM_011538750.2	2726	UTR 3			XP_011537052.1
XM_011538752.2	2726	UTR 3			XP_011537054.1
XM_017019978.1	2726	Intron			XP_016875467.1

Gene: TPCN1
Gene Name: two pore segment channel 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143819.2	2726	Intron			NP_001137291.1
NM_001301214.1	2726	Intron			NP_001288143.1
NM_017901.5	2726	Intron			NP_060371.2
XM_005253906.4	2726	Intron			XP_005253963.1
XM_011538490.2	2726	Intron			XP_011536792.1
XM_011538492.2	2726	Intron			XP_011536794.1
XM_011538493.2	2726	Intron			XP_011536795.1
XM_017019480.1	2726	Intron			XP_016874969.1
XM_017019481.1	2726	Intron			XP_016874970.1
XM_017019482.1	2726	Intron			XP_016874971.1

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