Product Details

SNP ID
rs4463569
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:5897342 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCACTGAGCACCTGAATTTCATTGA[C/T]CAGCTTGGACGAACCCTTTTTCTCC
Phenotype
MIM: 300427
Polymorphism
C/T, Transition 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 Intron NP_001269074.1
NM_001282146.1 Intron NP_001269075.1
NM_020742.3 Intron NP_065793.1
NM_181332.2 Intron NP_851849.1
XM_005274564.2 Intron XP_005274621.1
XM_005274565.2 Intron XP_005274622.1
XM_005274566.4 Intron XP_005274623.1
XM_006724504.3 Intron XP_006724567.1
XM_011545547.2 Intron XP_011543849.1
XM_011545548.2 Intron XP_011543850.1
XM_017029690.1 Intron XP_016885179.1
XM_017029691.1 Intron XP_016885180.1
XM_017029692.1 Intron XP_016885181.1
XM_017029693.1 Intron XP_016885182.1

View Full Product Details