rs537644349 Rat Genome Database

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Variant: rs537644349 -  Homo sapiens

RGD ID: 150440414
RS ID: rs537644349
ClinVar ID: CV1201684
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C19orf12  LOC130064129  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 30,206,156
GRCh38 19 29,715,249
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001256047.2:c.-11+314G>A
NM_001256046.3:c.-135G>A
NM_031448.6:c.-135G>A
NC_000019.10:g.29715249C>T
More... 		03/06/2019 5 prime utr variant likely benign none provided

Gene Symbol:C19orf12
Accession:NM_001256046
Location:5UTRS;EXON

Gene Symbol:C19orf12
Accession:NM_001282930
Location:5UTRS;EXON

Gene Symbol:C19orf12
Accession:NM_031448
Location:5UTRS;EXON

Gene Symbol:C19orf12
Accession:NM_001282931
Location:5UTRS;EXON

Gene Symbol:C19orf12
Accession:NM_001256047
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:XM_024451734
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_047439496
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_047439497
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_001282929
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_001031726
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_024451735
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001583496 CLINVAR
dbSNP (RS) rs537644349 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C19orf12 CLINVAR
  LOC130064129 CLINVAR
OMIM 614297 CLINVAR