Product Details

SNP ID

rs647152

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:64341646 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGTGCTGGCACTGTCTGGGCCAGA[G/T]CCTGGGGAGCTGGCACCTGCCGAGC

Phenotype

MIM: 611205

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

CCDC88B PubMed Links

Gene Details

Gene

CCDC88B

Gene Name

coiled-coil domain containing 88B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032251.5	641	Missense Mutation	GAG,GAT	E193D	NP_115627.6
XM_006718519.3	641	Missense Mutation	GAG,GAT	E193D	XP_006718582.1
XM_011544957.2	641	Missense Mutation	GAG,GAT	E193D	XP_011543259.1
XM_011544959.2	641	Missense Mutation	GAG,GAT	E193D	XP_011543261.1
XM_011544960.2	641	Missense Mutation	GAG,GAT	E193D	XP_011543262.1
XM_011544962.2	641	Intron			XP_011543264.1
XM_017017601.1	641	Missense Mutation	GAG,GAT	E193D	XP_016873090.1

Gene

MIR7155

Gene Name

microRNA 7155

There are no transcripts associated with this gene.

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