Product Details

SNP ID

rs202192382

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:64728916 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGGGGCAGAGAGAAGCTGAAGGCG[A/C]GGTGATGGTGGCTGTGCATGGGTGA

Phenotype

MIM: 600566 MIM: 605577

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

NRXN2 PubMed Links

Gene Details

Gene

NRXN2

Gene Name

neurexin 2

There are no transcripts associated with this gene.

Gene

RASGRP2

Gene Name

RAS guanyl releasing protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098670.1	2296	Missense Mutation	CGC,CTC	R573L	NP_001092140.1
NM_001098671.1	2296	Missense Mutation	CGC,CTC	R573L	NP_001092141.1
NM_001318398.1	2296	Missense Mutation	CGC,CTC	R428L	NP_001305327.1
NM_153819.1	2296	Missense Mutation	CGC,CTC	R573L	NP_722541.1
XM_005273707.3	2296	Missense Mutation	CGC,CTC	R678L	XP_005273764.3
XM_011544718.1	2296	Missense Mutation	CGC,CTC	R678L	XP_011543020.1
XM_011544720.1	2296	Missense Mutation	CGC,CTC	R573L	XP_011543022.1
XM_011544721.1	2296	Missense Mutation	CGC,CTC	R573L	XP_011543023.1
XM_011544722.1	2296	Missense Mutation	CGC,CTC	R573L	XP_011543024.1
XM_011544723.2	2296	Missense Mutation	CGC,CTC	R573L	XP_011543025.1
XM_011544725.2	2296	Missense Mutation	CGC,CTC	R428L	XP_011543027.1
XM_017017082.1	2296	Missense Mutation	CGC,CTC	R861L	XP_016872571.1
XM_017017083.1	2296	Missense Mutation	CGC,CTC	R861L	XP_016872572.1
XM_017017084.1	2296	Missense Mutation	CGC,CTC	R573L	XP_016872573.1
XM_017017085.1	2296	Missense Mutation	CGC,CTC	R514L	XP_016872574.1
XM_017017086.1	2296	Missense Mutation	CGC,CTC	R428L	XP_016872575.1

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