Variant #0000719079 (NC_000002.11:g.85893771_85893772insTT, NM_198843.2:c.397_398insAA (SFTPB))

Chromosome 2
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.85893771_85893772insTT
DNA change (hg38) -
Published as SFTPB(NM_198843.2):c.397_398insAA (p.P133Qfs*95), SFTPB(NM_198843.3):c.361_362insAA (p.P121Qfs*95)
ISCN -
DB-ID SFTPB_000009 See all 2 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) 0.00023 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SFTPB NM_000542.3 +/. - c.397_398insAA r.(?) p.(Pro133Glnfs*95)
SFTPB NM_198843.2 +/. - c.397_398insAA r.(?) p.(Pro133Glnfs*95)


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