Variant #0000266728 (NC_000007.13:g.117149185_117149186del, NM_000492.3:c.262_263del (CFTR))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.117149185_117149186del
DNA change (hg38) g.117509131_117509132del
Published as CFTR(NM_000492.3):c.262_263delTT (p.L88Ifs*22), CFTR(NM_000492.4):c.262_263delTT (p.L88Ifs*22)
ISCN -
DB-ID CFTR_000027 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFTR NM_000492.3 +/. - c.262_263del r.(?) p.(Leu88IlefsTer22)


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