Variant #0000536540 (NC_000009.11:g.133729620T>G, ABL1(NM_007313.2):c.306T>G)

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.133729620T>G
DNA change (hg38) g.130854233T>G
Published as ABL1(NM_005157.5):c.249T>G (p.T83=), ABL1(NM_007313.2):c.306T>G (p.T102=)
ISCN -
DB-ID ABL1_000011 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) 0.00647 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABL1 NM_005157.4 -/. - c.249T>G r.(?) p.(Thr83=)
ABL1 NM_007313.2 -/. - c.306T>G r.(?) p.(Thr102=)