RGD:14742374 Rat Genome Database

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Variant: RGD:14742374 -  Homo sapiens

RGD ID: 14742374
RS ID: rs1306471349
ClinVar ID: CV665814
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ANO5  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 22,242,624
GRCh38 11 22,221,078
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001142649.2:c.178-19T>C
NG_015844.1:g.32903T>C
NC_000011.10:g.22221078T>C
NC_000011.9:g.22242624T>C
More...
04/04/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ANO5
Accession:NM_001142649
Location:INTRON

Gene Symbol:ANO5
Accession:XM_011519949
Location:INTRON

Gene Symbol:ANO5
Accession:NM_001410963
Location:INTRON

Gene Symbol:ANO5
Accession:NM_001410964
Location:INTRON

Gene Symbol:ANO5
Accession:NM_213599
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ANO5
Accession:XM_047426522
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ANO5
Accession:XM_005252822
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000841344 CLINVAR
dbSNP (RS) rs1306471349 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene ANO5 CLINVAR
OMIM 608662 CLINVAR