Product Details

SNP ID

rs201815857

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:155187722 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGCAGCCAGGGAAGTAGCCTCAC[C/T]GCTGACGTCTGAGATCGTCAGGTTA

Phenotype

MIM: 158340 MIM: 188062 MIM: 600986

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MIR92B PubMed Links

Gene Details

Gene

MIR92B

Gene Name

microRNA 92b

There are no transcripts associated with this gene.

Gene

MUC1

Gene Name

mucin 1, cell surface associated

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001018016.2	418	Missense Mutation	ATG,GTG	M150V	NP_001018016.1
NM_001018017.2	418	Missense Mutation	ATG,GTG	M141V	NP_001018017.1
NM_001044390.2	418	Intron			NP_001037855.1
NM_001044391.2	418	Intron			NP_001037856.1
NM_001044392.2	418	Intron			NP_001037857.1
NM_001044393.2	418	Intron			NP_001037858.1
NM_001204285.1	418	Missense Mutation	ATG,GTG	M361V	NP_001191214.1
NM_001204286.1	418	Missense Mutation	ATG,GTG	M370V	NP_001191215.1
NM_001204287.1	418	Missense Mutation	ATG,GTG	M168V	NP_001191216.1
NM_001204288.1	418	Missense Mutation	ATC,GTC	I150V	NP_001191217.1
NM_001204289.1	418	Missense Mutation	ATG,GTG	M124V	NP_001191218.1
NM_001204290.1	418	Missense Mutation	ATG,GTG	M103V	NP_001191219.1
NM_001204291.1	418	Missense Mutation	ATG,GTG	M127V	NP_001191220.1
NM_001204292.1	418	Missense Mutation	ATG,GTG	M125V	NP_001191221.1
NM_001204293.1	418	Missense Mutation	AGC,GGC	S159G	NP_001191222.1
NM_001204294.1	418	Missense Mutation	ATG,GTG	M116V	NP_001191223.1
NM_001204295.1	418	Intron			NP_001191224.1
NM_001204296.1	418	Intron			NP_001191225.1
NM_001204297.1	418	Intron			NP_001191226.1
NM_002456.5	418	Missense Mutation	ATG,GTG	M159V	NP_002447.4

Gene

THBS3

Gene Name

thrombospondin 3

There are no transcripts associated with this gene.

Gene

TRIM46

Gene Name

tripartite motif containing 46

There are no transcripts associated with this gene.

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