Product Details

SNP ID

rs142722847

Assay Type

Functionally tested

NCBI dbSNP Submissions

10

Location

Chr.1:155197469 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATCTGAGCAGCTGGGGACCTTGAG[A/C]TGCAGCCCGGGCTGGGCAACCGCCC

Phenotype

MIM: 158340 MIM: 188062

Polymorphism

A/C, Transversion 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

There are no transcripts associated with this gene.

Gene

THBS3

Gene Name

thrombospondin 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001252607.1	2549	Missense Mutation	CAG,CAT	Q822H	NP_001239536.1
NM_001252608.1	2549	Missense Mutation	CAG,CAT	Q711H	NP_001239537.1
NM_007112.4	2549	Missense Mutation	CAG,CAT	Q831H	NP_009043.1
XM_006711498.3	2549	Missense Mutation	CAG,CAT	Q888H	XP_006711561.1
XM_011509926.2	2549	Missense Mutation	CAG,CAT	Q891H	XP_011508228.1
XM_011509927.2	2549	Missense Mutation	CAG,CAT	Q882H	XP_011508229.1
XM_011509928.2	2549	Missense Mutation	CAG,CAT	Q860H	XP_011508230.1
XM_011509929.1	2549	Missense Mutation	CAG,CAT	Q834H	XP_011508231.1
XM_011509930.2	2549	Missense Mutation	CAG,CAT	Q891H	XP_011508232.1
XM_011509931.1	2549	Missense Mutation	CAG,CAT	Q796H	XP_011508233.1
XM_011509932.2	2549	Missense Mutation	CAG,CAT	Q796H	XP_011508234.1
XM_011509933.1	2549	Missense Mutation	CAG,CAT	Q796H	XP_011508235.1
XM_011509934.1	2549	Missense Mutation	CAG,CAT	Q655H	XP_011508236.1
XM_011509935.1	2549	Missense Mutation	CAG,CAT	Q655H	XP_011508237.1
XM_011509936.1	2549	Missense Mutation	CAG,CAT	Q579H	XP_011508238.1
XM_017002206.1	2549	Missense Mutation	CAG,CAT	Q363H	XP_016857695.1

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