RGD:11651847 Rat Genome Database

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Variant: RGD:11651847 -  Homo sapiens

RGD ID: 11651847
RS ID: rs202136352
ClinVar ID: CV286773
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRXN1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 50,148,462
GRCh38 2 49,921,324
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_011878.1:g.1116213A>T
NC_000002.12:g.49921324T>A
NC_000002.11:g.50148462T>A
NM_001135659.1:c.*620A>T
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:NRXN1
Accession:NM_001320157
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330094
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330083
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330077
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330085
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330086
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330087
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330082
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_138735
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330084
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_004801
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001320156
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330093
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330092
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330095
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330097
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330096
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001135659
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330078
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330091
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330088
Location:3UTRS;EXON

Gene Symbol:NRXN1
Accession:NM_001330081
Location:INTRON

Gene Symbol:NRXN1
Accession:NM_001330090
Location:INTRON

Gene Symbol:NRXN1
Accession:NM_001330079
Location:INTRON

Gene Symbol:NRXN1
Accession:NM_001330089
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000301131 CLINVAR
dbSNP (RS) rs202136352 CLINVAR
MedGen C3280479 CLINVAR
NCBI Gene NRXN1 CLINVAR
OMIM 600565 CLINVAR
  614325 CLINVAR