Product Details

SNP ID

rs3810687

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.X:5892643 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TAATACTGGAAAACACCAACGATAA[T/G]GGTCTGCCGGGATGGGATGACTGCC

Phenotype

MIM: 300427

Polymorphism

T/G, Transversion substitution

Allele Nomenclature

Literature Links

NLGN4X PubMed Links

Gene Details

Gene

NLGN4X

Gene Name

neuroligin 4, X-linked

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282145.1	3309	Intron			NP_001269074.1
NM_001282146.1	3309	UTR 3			NP_001269075.1
NM_020742.3	3309	Intron			NP_065793.1
NM_181332.2	3309	Intron			NP_851849.1
XM_005274564.2	3309	Intron			XP_005274621.1
XM_005274565.2	3309	UTR 3			XP_005274622.1
XM_005274566.4	3309	Intron			XP_005274623.1
XM_006724504.3	3309	UTR 3			XP_006724567.1
XM_011545547.2	3309	UTR 3			XP_011543849.1
XM_011545548.2	3309	Intron			XP_011543850.1
XM_017029690.1	3309	UTR 3			XP_016885179.1
XM_017029691.1	3309	UTR 3			XP_016885180.1
XM_017029692.1	3309	Intron			XP_016885181.1
XM_017029693.1	3309	UTR 3			XP_016885182.1

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