Variant #0001024465 (NC_000002.11:g.203332393del, NM_001204.6:c.399del (BMPR2))

Chromosome 2
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.203332393del
DNA change (hg38) -
Published as BMPR2(NM_001204.6):c.399delT (p.P134Lfs*18), BMPR2(NM_001204.7):c.399delT (p.P134Lfs*18)
ISCN -
DB-ID BMPR2_000037 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) 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 2025-02-07 18:57:27 +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     
BMPR2 NM_001204.6 +/. - c.399del r.(?) p.(Pro134Leufs*18)


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