Variant #0000862004 (NC_000010.10:g.81318748C>T, NM_001098668.2:c.186G>A (SFTPA2))

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.81318748C>T
DNA change (hg38) -
Published as SFTPA2(NM_001098668.4):c.186G>A (p.P62=), SFTPA2(NM_001320814.1):c.216G>A (p.P72=)
ISCN -
DB-ID SFTPA2_000015 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) 0.00171 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SFTPA2 NM_001098668.2 -/. - c.186G>A r.(?) p.(Pro62=)


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