Genomic variant #0000184526

Individual ID 00114729
Chromosome X
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification -
DNA change (genomic) (Relative to hg19 / GRCh37) g.2876381A>C
DNA change (hg38) g.2958340A>C
Published as -
ISCN -
DB-ID ARSE_000022 See all 3 reported entries
Variant remarks -
Reference PubMed: Nino 2008
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Claudia Matos-Miranda
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSE NM_000047.2 +/. 3 c.119T>G r.(?) p.(I40S)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000115186 DNA SEQ - - ARSE 1 Claudia Matos-Miranda