RGD:25320722 Rat Genome Database

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Variant: RGD:25320722 -  Homo sapiens

RGD ID: 25320722
RS ID: rs1383104098
ClinVar ID: CV817863
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARVCF  COMT  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 19,957,152
GRCh38 22 19,969,629
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1010:g.32890C>T
NM_001135161.2:c.*893C>T
NG_023326.1:g.52158G>A
NM_001135162.2:c.*893C>T
More...
04/28/2018 3 prime utr variant drug response Ultram response

Variant Details
Variant Transcripts
Gene Symbol:COMT
Accession:NM_000754
Location:3UTRS;EXON

Gene Symbol:COMT
Accession:NM_001135161
Location:3UTRS;EXON

Gene Symbol:COMT
Accession:NM_001135162
Location:3UTRS;EXON

Gene Symbol:COMT
Accession:NM_007310
Location:3UTRS;EXON

Gene Symbol:COMT
Accession:NM_001362828
Location:3UTRS;EXON

Gene Symbol:ARVCF
Accession:NM_001670
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_005261242
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_005261244
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_006724243
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_006724246
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_006724245
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_011530179
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_011530182
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_011530180
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_011530181
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_047441371
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_047441370
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_047441369
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_047441368
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_047441367
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_047441375
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_047441373
Location:INTRON

Gene Symbol:ARVCF
Accession:XM_047441372
Location:INTRON

Gene Symbol:ARVCF
Accession:NM_001410839
Location:INTRON

Gene Symbol:ARVCF
Accession:XR_007067973
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001028846 CLINVAR
dbSNP (RS) rs1383104098 CLINVAR
MedGen CN078023 CLINVAR
NCBI Gene ARVCF CLINVAR
  COMT CLINVAR
OMIM 116790 CLINVAR
  602269 CLINVAR