Variant #0000978442 (NC_000009.11:g.133738171C>T, NM_007313.2:c.628C>T (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.133738171C>T
DNA change (hg38) -
Published as ABL1(NM_005157.4):c.571C>T (p.(Arg191Cys)), ABL1(NM_005157.6):c.571C>T (p.R191C)
ISCN -
DB-ID ABL1_000066 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) 4.0E-5 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.571C>T r.(?) p.(Arg191Cys)
ABL1 NM_007313.2 ?/. - c.628C>T r.(?) p.(Arg210Cys)


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