Variant #0000861183 (NC_000008.10:g.22020609T>C, NM_006129.4:c.-2310T>C (BMP1))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.22020609T>C
DNA change (hg38) -
Published as SFTPC(NM_003018.4):c.218T>C (p.I73T)
ISCN -
DB-ID SFTPC_000001 See all 17 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.218T>C r.(?) p.(Ile73Thr)
BMP1 NM_006129.4 +/. - c.-2310T>C r.(?) p.(=)


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