Variant #0000803911 (NC_000009.11:g.133759378C>T, NM_007313.2:c.1758C>T (ABL1))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.133759378C>T
DNA change (hg38) -
Published as ABL1(NM_005157.6):c.1701C>T (p.A567=), ABL1(NM_007313.2):c.1758C>T (p.A586=)
ISCN -
DB-ID ABL1_000047 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00193 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABL1 NM_005157.4 -/. - c.1701C>T r.(?) p.(Ala567=)
ABL1 NM_007313.2 -/. - c.1758C>T r.(?) p.(Ala586=)


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