Variant #0000978443 (NC_000009.11:g.133738340A>G, NM_007313.2:c.797A>G (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.133738340A>G |
DNA change (hg38) |
- |
Published as |
ABL1(NM_005157.6):c.740A>G (p.(Lys247Arg), p.K247R), ABL1(NM_007313.2):c.797A>G (p.K266R), ABL1(NM_007313.3):c.797A>G (p.K266R) |
ISCN |
- |
DB-ID |
ABL1_000014 See all 4 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) |
0.00259 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
|