Variant #0000889268 (NC_000010.10:g.81371164A>G, NC_000010.10(NM_005411.4):c.-24+19A>G (SFTPA1))

Chromosome 10
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.81371164A>G
DNA change (hg38) -
Published as SFTPA1(NM_005411.5):c.-24+19A>G
ISCN -
DB-ID SFTPA1_000014
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SFTPA1 NM_001093770.2 -/. - c.-38-174A>G r.(=) p.(=)
SFTPA1 NM_005411.4 -/. - c.-24+19A>G r.(=) p.(=)


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