Variant #0000690435 (NC_000009.11:g.133759793G>A, NM_007313.2:c.2173G>A (ABL1))

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.133759793G>A
DNA change (hg38) -
Published as ABL1(NM_005157.4):c.2116G>A (p.(Gly706Ser)), ABL1(NM_007313.2):c.2173G>A (p.G725S)
ISCN -
DB-ID ABL1_000039 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) 0.00257 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABL1 NM_005157.4 -/. - c.2116G>A r.(?) p.(Gly706Ser)
ABL1 NM_007313.2 -/. - c.2173G>A r.(?) p.(Gly725Ser)


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