Variant #0000513953 (NC_000002.11:g.203383771_203383772insATA, NM_001204.6:c.848_849insATA (BMPR2))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.203383771_203383772insATA
DNA change (hg38) g.202519048_202519049insATA
Published as BMPR2(NM_001204.7):c.848_849insATA (p.P283_N284insY)
ISCN -
DB-ID BMPR2_000016
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMPR2 NM_001204.6 ?/. - c.848_849insATA r.(?) p.(Pro283_Asn284insTyr)


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