Product Details

SNP ID

rs1662986

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:26581783 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGAGAGGGGCCACCCAGGCCACAG[C/G]CCCTAGCAGGCCTGTTGGAATGAGG

Phenotype

MIM: 610646

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C2orf70 PubMed Links

Gene Details

Gene

C2orf70

Gene Name

chromosome 2 open reading frame 70

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001105519.2		Intron			NP_001098989.1
NM_001322426.1		Intron			NP_001309355.1
XM_011532810.2		Intron			XP_011531112.1
XM_011532811.2		Intron			XP_011531113.1
XM_017003962.1		Intron			XP_016859451.1
XM_017003963.1		Intron			XP_016859452.1
XM_017003964.1		Intron			XP_016859453.1
XM_017003965.1		Intron			XP_016859454.1
XM_017003966.1		Intron			XP_016859455.1

Gene

CIB4

Gene Name

calcium and integrin binding family member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001029881.2		Intron			NP_001025052.1
XM_011532514.2		Intron			XP_011530816.1
XM_011532517.2		Intron			XP_011530819.1
XM_017003329.1		Intron			XP_016858818.1
XM_017003330.1		Intron			XP_016858819.1
XM_017003331.1		Intron			XP_016858820.1

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