Variant #0000162949 (NC_000008.10:g.22021060G>A, NC_000008.10(NM_003018.3):c.435+1G>A (SFTPC))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.22021060G>A
DNA change (hg38) g.22163547G>A
Published as -
ISCN -
DB-ID SFTPC_000007 See all 2 reported entries
Variant remarks consequences on splicing determined using a mini-gene construct
Reference Fanen, submitted
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Pascale Fanen
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Pascale Fanen
Date created 2017-02-07 17:43:55 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SFTPC NM_003018.3 +/. 4i c.435+1G>A r.325_435del p.Leu109_Gln145del


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