Variant #0001072414 (NC_000009.11:g.133589843G>A, NC_000009.11(NM_007313.2):c.136+1G>A (ABL1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.133589843G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ABL1_000079
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2490826872
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-10 15:52:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABL1 NM_007313.2 ?/. - c.136+1G>A r.(?) p.(?)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.