Product Details

SNP ID

rs201640492

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.Y:14622211 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCAATGTTCTTCTGTGGATAACTG[C/T]TCTTGCCATCAAGTTCACCCTCATT

Phenotype

MIM: 400028

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NLGN4Y PubMed Links

Gene Details

Gene

NLGN4Y

Gene Name

neuroligin 4, Y-linked

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001164238.1	321	Missense Mutation	GCT,GTT	A31V	NP_001157710.1
NM_001206850.1	321	Intron			NP_001193779.1
NM_014893.4	321	Missense Mutation	GCT,GTT	A31V	NP_055708.3
XM_006724874.2	321	Missense Mutation	GCT,GTT	A31V	XP_006724937.1
XM_011531424.2	321	Missense Mutation	GCT,GTT	A31V	XP_011529726.1
XM_011531425.2	321	Missense Mutation	GCT,GTT	A31V	XP_011529727.1
XM_011531426.2	321	Missense Mutation	GCT,GTT	A31V	XP_011529728.1
XM_011531427.1	321	Missense Mutation	GCT,GTT	A31V	XP_011529729.1
XM_011531428.1	321	Missense Mutation	GCT,GTT	A31V	XP_011529730.1
XM_011531429.2	321	Missense Mutation	GCT,GTT	A31V	XP_011529731.1
XM_011531430.2	321	Missense Mutation	GCT,GTT	A31V	XP_011529732.1
XM_017030034.1	321	Missense Mutation	GCT,GTT	A31V	XP_016885523.1
XM_017030035.1	321	Intron			XP_016885524.1
XM_017030036.1	321	Missense Mutation	GCT,GTT	A31V	XP_016885525.1
XM_017030037.1	321	Missense Mutation	GCT,GTT	A31V	XP_016885526.1
XM_017030038.1	321	Missense Mutation	GCT,GTT	A31V	XP_016885527.1
XM_017030039.1	321	Intron			XP_016885528.1
XM_017030040.1	321	Intron			XP_016885529.1
XM_017030041.1	321	Missense Mutation	GCT,GTT	A31V	XP_016885530.1

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