Variant #0000298162 (NC_000008.10:g.22021517G>A, NM_006129.4:c.-1402G>A (BMP1))

Chromosome 8
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.22021517G>A
DNA change (hg38) g.22164004G>A
Published as SFTPC(NM_001172357.2):c.539G>A (p.S180N)
ISCN -
DB-ID SFTPC_000021
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) 0.29805 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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SFTPC NM_003018.3 -/. - c.557G>A r.(?) p.(Ser186Asn)
BMP1 NM_006129.4 -/. - c.-1402G>A r.(?) p.(=)


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