Variant #0000003052 (NC_000009.12:g.130874969A>C, NM_005157.5:c.1187A>C (ABL1))

Individual ID 00000781
Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.130874969A>C
Published as -
Reference N S Jamali et al.(2021)
DB-ID ABL1_000001
dbSNP ID rs1396443734
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-07-13 12:01:47 +08:00 (CST)
Date last edited 2021-09-08 16:01:35 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
ABL1 NM_005157.5 +/. - c.1187A>C - r.(?) p.(His396Pro) missense -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000875 RNA PFGE;RT-PCR;SEQ ABL1 1 Nur Aisyah Athirah