Product Details

SNP ID

rs201776185

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:89949630 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGGTCACGCCGCGGGCAGGACGCG[G/T]GAGGCCAGGTCCGTGCATCCCGCGT

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

DEF8 PubMed Links

Gene Details

Gene

DEF8

Gene Name

differentially expressed in FDCP 8 homolog (mouse)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242816.1	231	Intron			NP_001229745.1
NM_001242817.1	231	Intron			NP_001229746.1
NM_001242818.1	231	Intron			NP_001229747.1
NM_001242819.1	231	Intron			NP_001229748.1
NM_001242820.1	231	Intron			NP_001229749.1
NM_001242821.1	231	Intron			NP_001229750.1
NM_001242822.1	231	Intron			NP_001229751.1
NM_017702.3	231	Intron			NP_060172.1
NM_207514.2	231	Intron			NP_997397.1
XM_005256318.2	231	Intron			XP_005256375.2
XM_011523156.2	231	Intron			XP_011521458.1
XM_011523157.2	231	Intron			XP_011521459.1
XM_011523158.1	231	Intron			XP_011521460.1
XM_011523159.2	231	Silent Mutation	CGG,CGT	R28R	XP_011521461.1
XM_011523160.2	231	Silent Mutation	CGG,CGT	R55R	XP_011521462.1
XM_011523161.2	231	Silent Mutation	CGG,CGT	R55R	XP_011521463.1
XM_011523162.2	231	Intron			XP_011521464.1
XM_017023358.1	231	Intron			XP_016878847.1
XM_017023359.1	231	Intron			XP_016878848.1
XM_017023360.1	231	Intron			XP_016878849.1
XM_017023361.1	231	Intron			XP_016878850.1
XM_017023362.1	231	Intron			XP_016878851.1
XM_017023363.1	231	Intron			XP_016878852.1
XM_017023364.1	231	Intron			XP_016878853.1
XM_017023365.1	231	Intron			XP_016878854.1
XM_017023366.1	231	Intron			XP_016878855.1
XM_017023367.1	231	Intron			XP_016878856.1
XM_017023368.1	231	Intron			XP_016878857.1
XM_017023369.1	231	Intron			XP_016878858.1

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