Variant #0000298157 (NC_000002.11:g.85893741G>A, NM_198843.2:c.428C>T (SFTPB))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.85893741G>A
DNA change (hg38) g.85666618G>A
Published as SFTPB(NM_000542.5):c.392C>T (p.T131I)
ISCN -
DB-ID SFTPB_000003
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) 0.49544 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 2018-01-15 20:58:59 +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.428C>T r.(?) p.(Thr143Ile)
SFTPB NM_198843.2 -/. - c.428C>T r.(?) p.(Thr143Ile)


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