RGD:150495220 Rat Genome Database

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Variant: RGD:150495220 -  Homo sapiens

RGD ID: 150495220
RS ID: rs73706437
ClinVar ID: CV1266191
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL14A1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 121,344,750
GRCh38 8 120,332,511
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001384947.1:c.4714-153G>A
NM_021110.4:c.4714-153G>A
NG_033107.1:g.212404G>A
NC_000008.11:g.120332511G>A
More... 		06/19/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:COL14A1
Accession:NM_021110
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001384947
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413490
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413491
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413493
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413498
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413494
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413492
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413495
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413496
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413497
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413499
Location:INTRON

Gene Symbol:COL14A1
Accession:NM_001413500
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001688513 CLINVAR
dbSNP (RS) rs73706437 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL14A1 CLINVAR
OMIM 120324 CLINVAR