Variant #0000690433 (NC_000009.11:g.133759686A>G, NM_007313.2:c.2066A>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.133759686A>G
DNA change (hg38) -
Published as ABL1(NM_005157.6):c.2009A>G (p.N670S), ABL1(NM_007313.2):c.2066A>G (p.N689S), ABL1(NM_007313.3):c.2066A>G (p.N689S)
ISCN -
DB-ID ABL1_000043 See all 3 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) 0.00037 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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.2009A>G r.(?) p.(Asn670Ser)
ABL1 NM_007313.2 -?/. - c.2066A>G r.(?) p.(Asn689Ser)


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