rs377152944 Rat Genome Database

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Variant: rs377152944 -  Homo sapiens

RGD ID: 11094217
RS ID: rs377152944
ClinVar ID: CV231255
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DMD  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 31,284,952
GRCh38 X 31,266,835
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_199:g.2077775G>T
NG_012232.1:g.2077775G>T
NC_000023.11:g.31266835C>A
NC_000023.10:g.31284952C>A
More...
03/21/2024 5 prime utr variant|intron variant likely benign|uncertain significance AllHighlyPenetrant; DMD-related condition

Variant Details
Variant Transcripts
Gene Symbol:DMD
Accession:NM_004017
Location:5UTRS;EXON

Gene Symbol:DMD
Accession:NM_004016
Location:5UTRS;EXON

Gene Symbol:DMD
Accession:NM_004019
Location:5UTRS;EXON

Gene Symbol:DMD
Accession:NM_004015
Location:5UTRS;EXON

Gene Symbol:DMD
Accession:NM_004018
Location:5UTRS;EXON

Gene Symbol:DMD
Accession:NM_004010
Location:INTRON

Gene Symbol:DMD
Accession:NM_004013
Location:INTRON

Gene Symbol:DMD
Accession:XM_006724469
Location:INTRON

Gene Symbol:DMD
Accession:XM_011545467
Location:INTRON

Gene Symbol:DMD
Accession:XM_017029330
Location:INTRON

Gene Symbol:DMD
Accession:NM_004012
Location:INTRON

Gene Symbol:DMD
Accession:XM_017029329
Location:INTRON

Gene Symbol:DMD
Accession:NM_004009
Location:INTRON

Gene Symbol:DMD
Accession:XM_011545469
Location:INTRON

Gene Symbol:DMD
Accession:XM_047441889
Location:INTRON

Gene Symbol:DMD
Accession:XM_006724474
Location:INTRON

Gene Symbol:DMD
Accession:XM_006724470
Location:INTRON

Gene Symbol:DMD
Accession:NM_004021
Location:INTRON

Gene Symbol:DMD
Accession:XM_017029328
Location:INTRON

Gene Symbol:DMD
Accession:NM_004006
Location:INTRON

Gene Symbol:DMD
Accession:XM_011545468
Location:INTRON

Gene Symbol:DMD
Accession:NM_004023
Location:INTRON

Gene Symbol:DMD
Accession:NM_004022
Location:INTRON

Gene Symbol:DMD
Accession:XM_006724473
Location:INTRON

Gene Symbol:DMD
Accession:NM_004020
Location:INTRON

Gene Symbol:DMD
Accession:NM_000109
Location:INTRON

Gene Symbol:DMD
Accession:NM_004011
Location:INTRON

Gene Symbol:DMD
Accession:NM_004014
Location:INTRON

Gene Symbol:DMD
Accession:XM_006724475
Location:INTRON

Gene Symbol:DMD
Accession:XM_006724468
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:24033266  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000220771 CLINVAR
  RCV004737341 CLINVAR
dbSNP (RS) rs377152944 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene DMD CLINVAR
OMIM 300377 CLINVAR