Product Details

SNP ID

rs201095031

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:141136720 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGGGCCTCCCGGGGCCCCCCAGAG[C/T]GCCAGAGCCTGAGGATGTCGCCGTC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

DENND3 PubMed Links

Gene Details

Gene

DENND3

Gene Name

DENN domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014957.2	338	Missense Mutation	GCG,GTG	A25V	NP_055772.2
XM_005250838.4	338	Missense Mutation	GCG,GTG	A38V	XP_005250895.2
XM_005250839.2	338	Missense Mutation	GCG,GTG	A38V	XP_005250896.2
XM_005250840.4	338	Missense Mutation	GCG,GTG	A38V	XP_005250897.2
XM_005250841.3	338	Missense Mutation	GCG,GTG	A38V	XP_005250898.2
XM_005250842.4	338	Missense Mutation	GCG,GTG	A105V	XP_005250899.1
XM_011516933.1	338	Missense Mutation	GCG,GTG	A38V	XP_011515235.1
XM_011516934.2	338	Missense Mutation	GCG,GTG	A38V	XP_011515236.1
XM_011516937.1	338	Missense Mutation	GCG,GTG	A38V	XP_011515239.1
XM_011516938.2	338	Intron			XP_011515240.1
XM_011516939.2	338	Intron			XP_011515241.1
XM_011516940.2	338	Intron			XP_011515242.1
XM_011516941.2	338	Missense Mutation	GCG,GTG	A38V	XP_011515243.1
XM_017013241.1	338	Missense Mutation	GCG,GTG	A38V	XP_016868730.1
XM_017013242.1	338	UTR 5			XP_016868731.1
XM_017013243.1	338	Intron			XP_016868732.1

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