Product Details

SNP ID

rs139255180

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:201649240 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGCCGCTCAGCAAGGCGCCTGAAG[C/T]GGCCGTGAGCGAAGATGGCAAATCG

Phenotype

MIM: 611628

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NAV1 PubMed Links

Gene Details

Gene

NAV1

Gene Name

neuron navigator 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001167738.1	598	Intron			NP_001161210.1
NM_020443.4	598	Missense Mutation	GCG,GTG	A191V	NP_065176.3
XM_006711609.2	598	Intron			XP_006711672.2
XM_006711610.2	598	Intron			XP_006711673.2
XM_006711611.1	598	Intron			XP_006711674.1
XM_011510097.1	598	Missense Mutation	GCG,GTG	A191V	XP_011508399.1
XM_011510098.1	598	Missense Mutation	GCG,GTG	A191V	XP_011508400.1
XM_011510099.1	598	Missense Mutation	GCG,GTG	A191V	XP_011508401.1
XM_011510100.1	598	Missense Mutation	GCG,GTG	A191V	XP_011508402.1
XM_011510101.1	598	Missense Mutation	GCG,GTG	A191V	XP_011508403.1
XM_011510102.1	598	Missense Mutation	GCG,GTG	A191V	XP_011508404.1
XM_017002751.1	598	Missense Mutation	GCG,GTG	A191V	XP_016858240.1
XM_017002752.1	598	Intron			XP_016858241.1
XM_017002753.1	598	Missense Mutation	GCG,GTG	A191V	XP_016858242.1
XM_017002754.1	598	Missense Mutation	GCG,GTG	A191V	XP_016858243.1

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