Variant #0000803912 (NC_000009.11:g.133759864G>A, NM_007313.2:c.2244G>A (ABL1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.133759864G>A
DNA change (hg38) -
Published as ABL1(NM_005157.6):c.2187G>A (p.T729=), ABL1(NM_007313.2):c.2244G>A (p.T748=)
ISCN -
DB-ID ABL1_000048 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) 0.00051 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABL1 NM_005157.4 -?/. - c.2187G>A r.(?) p.(Thr729=)
ABL1 NM_007313.2 -?/. - c.2244G>A r.(?) p.(Thr748=)


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