Variant #0000322718 (NC_000012.11:g.25362768_25362770del, KRAS(NM_004985.3):c.531_533del)

Chromosome 12
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.25362768_25362770del
DNA change (hg38) g.25209834_25209836del
Published as KRAS(NM_004985.3):c.531_533del (p.(Lys180del)), KRAS(NM_004985.5):c.531_533delGAA (p.K180del)
ISCN -
DB-ID KRAS_000017 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 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LYRM5 NM_001001660.2 -?/. - c.*5522_*5524del r.(=) p.(=)
KRAS NM_004985.3 -?/. - c.531_533del r.(?) p.(Lys180del)