Variant #0000570394 (NC_000020.10:g.6750882T>G, NM_001200.2:c.109T>G (BMP2))

Chromosome 20
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.6750882T>G
DNA change (hg38) g.6770235T>G
Published as BMP2(NM_001200.2):c.109T>G (p.(Ser37Ala)), BMP2(NM_001200.4):c.109T>G (p.S37A)
ISCN -
DB-ID BMP2_000003 See all 4 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) 0.02349 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
BMP2 NM_001200.2 -/. - c.109T>G r.(?) p.(Ser37Ala)


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