RGD:11614442 Rat Genome Database

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Variant: RGD:11614442 -  Homo sapiens

RGD ID: 11614442
ClinVar ID: CV343770
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PAFAH1B1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 17 2,586,474
GRCh38 17 2,683,180
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009799.1:g.94552G>A
NC_000017.11:g.2683180G>A
NC_000017.10:g.2586474G>A
NM_000430.4:c.*1378G>A
More...
06/14/2016 3 prime utr variant likely benign

Variant Details
Variant Transcripts
Gene Symbol:PAFAH1B1
Accession:NM_000430
Location:3UTRS;EXON

Gene Symbol:PAFAH1B1
Accession:XM_011523901
Location:3UTRS;EXON

Gene Symbol:PAFAH1B1
Accession:XM_011523902
Location:3UTRS;EXON

Gene Symbol:PAFAH1B1
Accession:XM_011523903
Location:3UTRS;EXON

Gene Symbol:PAFAH1B1
Accession:XM_017024701
Location:3UTRS;EXON

Gene Symbol:PAFAH1B1
Accession:XM_047436163
Location:3UTRS;EXON

Gene Symbol:PAFAH1B1
Accession:XM_047436164
Location:3UTRS;EXON

Gene Symbol:PAFAH1B1
Accession:XM_047436162
Location:3UTRS;EXON

Gene Symbol:PAFAH1B1
Accession:XM_017024703
Location:INTRON

Variant Samples