Product Details

SNP ID

rs147915600

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:173396139 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTCCCCGCCTATGATTTTCGGAGG[C/T]GATTGCTCACTTAGCTGAGGATCTG

Phenotype

MIM: 600568

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NLGN1 PubMed Links

Gene Details

Gene

NLGN1

Gene Name

neuroligin 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014932.3	211	Intron			NP_055747.1
XM_005247234.2	211	Intron			XP_005247291.1
XM_005247235.3	211	Intron			XP_005247292.1
XM_005247236.2	211	Intron			XP_005247293.1
XM_005247237.3	211	Intron			XP_005247294.1
XM_006713540.3	211	Intron			XP_006713603.1
XM_011512551.2	211	Intron			XP_011510853.1
XM_011512552.2	211	UTR 5			XP_011510854.1
XM_011512553.2	211	Intron			XP_011510855.1
XM_011512554.2	211	Intron			XP_011510856.1
XM_017005888.1	211	Intron			XP_016861377.1
XM_017005889.1	211	Intron			XP_016861378.1
XM_017005890.1	211	Intron			XP_016861379.1
XM_017005891.1	211	Intron			XP_016861380.1
XM_017005892.1	211	UTR 5			XP_016861381.1
XM_017005893.1	211	UTR 5			XP_016861382.1
XM_017005894.1	211	Intron			XP_016861383.1
XM_017005895.1	211	Intron			XP_016861384.1
XM_017005896.1	211	Intron			XP_016861385.1
XM_017005897.1	211	Intron			XP_016861386.1
XM_017005898.1	211	Intron			XP_016861387.1
XM_017005899.1	211	UTR 5			XP_016861388.1
XM_017005900.1	211	Intron			XP_016861389.1
XM_017005901.1	211	UTR 5			XP_016861390.1
XM_017005902.1	211	Intron			XP_016861391.1
XM_017005903.1	211	Intron			XP_016861392.1
XM_017005904.1	211	UTR 5			XP_016861393.1
XM_017005905.1	211	Intron			XP_016861394.1

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