Variant #0000997554 (NC_000009.11:g.133760106C>T, NM_007313.2:c.2486C>T (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.133760106C>T
DNA change (hg38) -
Published as ABL1(NM_005157.4):c.2429C>T (p.(Pro810Leu)), ABL1(NM_005157.6):c.2429C>T (p.P810L)
ISCN -
DB-ID ABL1_000035 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) 0.00541 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 2024-08-28 13:16:32 +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.2429C>T r.(?) p.(Pro810Leu)
ABL1 NM_007313.2 -?/. - c.2486C>T r.(?) p.(Pro829Leu)


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