RGD:150462280 Rat Genome Database

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Variant: RGD:150462280 -  Homo sapiens

RGD ID: 150462280
RS ID: rs79049502
ClinVar ID: CV1253350
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CPAMD8  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 17,039,073
GRCh38 19 16,928,263
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_015692.5:c.3145-29C>T
NG_054892.1:g.103556C>T
NC_000019.10:g.16928263G>A
NC_000019.9:g.17039073G>A
 05/11/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CPAMD8
Accession:XM_011527919
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_017026594
Location:INTRON

Gene Symbol:CPAMD8
Accession:NM_015692
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_047438612
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_011527921
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_011527925
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_011527920
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_011527917
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_011527923
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_047438613
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_011527918
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_011527922
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_011527924
Location:INTRON

Gene Symbol:CPAMD8
Accession:XM_047438614
Location:INTRON

Gene Symbol:CPAMD8
Accession:NR_147452
Location:INTRON;NON-CODING

Gene Symbol:CPAMD8
Accession:NR_165644
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001669679 CLINVAR
dbSNP (RS) rs79049502 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CPAMD8 CLINVAR
OMIM 608841 CLINVAR