Product Details

SNP ID

rs148631428

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:32633975 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTGGGTTTCTACTTCTACTGTTT[C/G]GAGGGGCTCCACTGTCCCAGTATCT

Phenotype

MIM: 615891

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

ZBTB8OS PubMed Links

Gene Details

Gene

ZBTB8OS

Gene Name

zinc finger and BTB domain containing 8 opposite strand

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308135.1	260	Missense Mutation	CAA,GAA	Q79E	NP_001295064.1
NM_001308136.1	260	Missense Mutation	CAA,GAA	Q86E	NP_001295065.1
NM_001308137.1	260	Missense Mutation	CAA,GAA	Q79E	NP_001295066.1
NM_001308138.1	260	Missense Mutation	CAA,GAA	Q17E	NP_001295067.1
NM_001308139.1	260	Missense Mutation	CAA,GAA	Q17E	NP_001295068.1
NM_001308140.1	260	Missense Mutation	CAA,GAA	Q17E	NP_001295069.1
NM_001308141.1	260	Missense Mutation	CAA,GAA	Q17E	NP_001295070.1
NM_178547.3	260	Missense Mutation	CAA,GAA	Q86E	NP_848642.1
XM_011541327.2	260	Missense Mutation	CAA,GAA	Q86E	XP_011539629.1
XM_011541328.1	260	Intron			XP_011539630.1
XM_011541329.2	260	Missense Mutation	CAA,GAA	Q38E	XP_011539631.1
XM_011541330.2	260	Missense Mutation	CAA,GAA	Q34E	XP_011539632.1
XM_011541334.2	260	Missense Mutation	CAA,GAA	Q17E	XP_011539636.1
XM_011541335.2	260	Intron			XP_011539637.1
XM_011541337.2	260	Intron			XP_011539639.1
XM_011541338.2	260	Missense Mutation	CAA,GAA	Q17E	XP_011539640.1
XM_017001134.1	260	Intron			XP_016856623.1
XM_017001135.1	260	Missense Mutation	CAA,GAA	Q86E	XP_016856624.1
XM_017001136.1	260	Intron			XP_016856625.1
XM_017001137.1	260	Intron			XP_016856626.1
XM_017001138.1	260	Missense Mutation	CAA,GAA	Q17E	XP_016856627.1

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