Variant #0000861182 (NC_000008.10:g.22019380G>A, NM_006129.4:c.-3539G>A (BMP1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.22019380G>A
DNA change (hg38) -
Published as SFTPC(NM_001172357.1):c.39G>A (p.P13=)
ISCN -
DB-ID SFTPC_000041
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
SFTPC NM_003018.3 -?/. - c.39G>A r.(?) p.(Pro13=)
BMP1 NM_006129.4 -?/. - c.-3539G>A r.(?) p.(=)


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