Variant #0000949202 (NC_000009.11:g.133730278A>G, NM_007313.2:c.401A>G (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.133730278A>G
DNA change (hg38) -
Published as ABL1(NM_005157.6):c.344A>G (p.Y115C)
ISCN -
DB-ID ABL1_000060
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABL1 NM_005157.4 ?/. - c.344A>G r.(?) p.(Tyr115Cys)
ABL1 NM_007313.2 ?/. - c.401A>G r.(?) p.(Tyr134Cys)


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