Variant #0001046960 (NC_000023.10:g.50653934_50653935del, NM_005448.2:c.151_152del (BMP15))

Chromosome X
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.50653934_50653935del
DNA change (hg38) -
Published as -
ISCN -
DB-ID BMP15_000029
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1308688249
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-07-15 09:08:01 +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     
BMP15 NM_005448.2 +/. - c.151_152del r.(?) p.(Glu51IlefsTer28)


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