Product Details

SNP ID

rs111625451

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:64607920 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCGGCCTGGCACGGGCCCCCAGAG[A/G]GCGGGCGGCGCGCGGCGGGCGGGGG

Phenotype

MIM: 600566 MIM: 607096

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NRXN2 PubMed Links

Gene Details

Gene

NRXN2

Gene Name

neurexin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015080.3	2775	Missense Mutation	CCC,CTC	P1472L	NP_055895.1
NM_138732.2	2775	Missense Mutation	CCC,CTC	P1402L	NP_620060.1
NM_138734.2	2775	Missense Mutation	CCC,CTC	P426L	NP_620063.1
XM_005274400.3	2775	Missense Mutation	CCC,CTC	P1465L	XP_005274457.1
XM_005274401.3	2775	Intron			XP_005274458.1
XM_005274402.3	2775	Intron			XP_005274459.1
XM_011545370.1	2775	Missense Mutation	CCC,CTC	P1475L	XP_011543672.1
XM_011545371.1	2775	Missense Mutation	CCC,CTC	P1474L	XP_011543673.1
XM_011545373.1	2775	Missense Mutation	CCC,CTC	P1468L	XP_011543675.1
XM_011545375.1	2775	Missense Mutation	CCC,CTC	P1460L	XP_011543677.1
XM_011545385.1	2775	Missense Mutation	CCC,CTC	P737L	XP_011543687.1
XM_017018563.1	2775	Missense Mutation	CCC,CTC	P1465L	XP_016874052.1
XM_017018564.1	2775	Missense Mutation	CCC,CTC	P1464L	XP_016874053.1
XM_017018565.1	2775	Missense Mutation	CCC,CTC	P1463L	XP_016874054.1
XM_017018566.1	2775	Missense Mutation	CCC,CTC	P1451L	XP_016874055.1
XM_017018567.1	2775	Missense Mutation	CCC,CTC	P1445L	XP_016874056.1
XM_017018568.1	2775	Missense Mutation	CCC,CTC	P1442L	XP_016874057.1
XM_017018569.1	2775	Missense Mutation	CCC,CTC	P1441L	XP_016874058.1
XM_017018570.1	2775	Intron			XP_016874059.1
XM_017018571.1	2775	Intron			XP_016874060.1
XM_017018572.1	2775	Missense Mutation	CCC,CTC	P1240L	XP_016874061.1
XM_017018573.1	2775	Intron			XP_016874062.1
XM_017018574.1	2775	Missense Mutation	CCC,CTC	P1230L	XP_016874063.1
XM_017018575.1	2775	Missense Mutation	CCC,CTC	P1229L	XP_016874064.1
XM_017018576.1	2775	Missense Mutation	CCC,CTC	P1056L	XP_016874065.1
XM_017018577.1	2775	Missense Mutation	CCC,CTC	P734L	XP_016874066.1
XM_017018578.1	2775	Intron			XP_016874067.1

Gene

SLC22A12

Gene Name

solute carrier family 22 member 12

There are no transcripts associated with this gene.

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