Variant #0000656246 (NC_000009.11:g.133759697C>T, ABL1(NM_007313.2):c.2077C>T)

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.133759697C>T
DNA change (hg38) g.130884310C>T
Published as ABL1(NM_007313.2):c.2077C>T (p.R693W)
ISCN -
DB-ID ABL1_000037
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) Variant not found in online data sets
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.2020C>T r.(?) p.(Arg674Trp)
ABL1 NM_007313.2 ?/. - c.2077C>T r.(?) p.(Arg693Trp)