rs77247635 Rat Genome Database

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Variant: rs77247635 -  Homo sapiens

RGD ID: 14742059
RS ID: rs77247635
ClinVar ID: CV668001
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACTC1  GJD2-DT  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 35,086,562
GRCh38 15 34,794,361
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005159.5:c.129+319T>G
NG_007553.1:g.6366T>G
NC_000015.10:g.34794361A>C
NC_000015.9:g.35086562A>C
More... 		06/14/2018 intron variant benign none provided

Gene Symbol:ACTC1
Accession:NM_005159
Location:INTRON

Gene Symbol:ACTC1
Accession:NM_001406483
Location:INTRON

Gene Symbol:ACTC1
Accession:NM_001406485
Location:INTRON

Gene Symbol:ACTC1
Accession:NM_001406484
Location:INTRON

Gene Symbol:ACTC1
Accession:XM_047432979
Location:INTRON

Gene Symbol:ACTC1
Accession:NM_001406482
Location:INTRON

Gene Symbol:GJD2-DT
Accession:NR_120329
Location:INTRON;NON-CODING

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Database
Acc Id
Source(s)
ClinVar RCV000841116 CLINVAR
dbSNP (RS) rs77247635 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene 101928174 CLINVAR
  ACTC1 CLINVAR
OMIM 102540 CLINVAR