Product Details

SNP ID
rs4995613
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:5892880 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TACTGTTTTGTCCTCCACTGAAGGT[T/G]TTAAAAGTGTGCAAAGGCTGCATCC
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 3072 Intron NP_001269074.1
NM_001282146.1 3072 Missense Mutation AAA,AAC K796N NP_001269075.1
NM_020742.3 3072 Intron NP_065793.1
NM_181332.2 3072 Intron NP_851849.1
XM_005274564.2 3072 Intron XP_005274621.1
XM_005274565.2 3072 Missense Mutation AAA,AAC K816N XP_005274622.1
XM_005274566.4 3072 Intron XP_005274623.1
XM_006724504.3 3072 Missense Mutation AAA,AAC K816N XP_006724567.1
XM_011545547.2 3072 Missense Mutation AAA,AAC K816N XP_011543849.1
XM_011545548.2 3072 Intron XP_011543850.1
XM_017029690.1 3072 Missense Mutation AAA,AAC K816N XP_016885179.1
XM_017029691.1 3072 Missense Mutation AAA,AAC K796N XP_016885180.1
XM_017029692.1 3072 Intron XP_016885181.1
XM_017029693.1 3072 Missense Mutation AAA,AAC K796N XP_016885182.1

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