Product Details

SNP ID

rs141451836

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:113299782 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAGCACTAAGCGGCTTCAGTCACA[C/T]GCTTTTCAGGTGAATCACTCCAAAT

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	2364	Missense Mutation	ATG,GTG	M389V	XP_006719670.1
XM_011538749.2	2364	Missense Mutation	ATG,GTG	M584V	XP_011537051.1
XM_011538750.2	2364	Missense Mutation	ATG,GTG	M528V	XP_011537052.1
XM_011538752.2	2364	Missense Mutation	ATG,GTG	M389V	XP_011537054.1
XM_017019978.1	2364	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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