Variant #0000258922 (NC_000002.11:g.158626980C>T, NM_001105.4:c.690G>A (ACVR1))

Chromosome 2
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.158626980C>T
DNA change (hg38) g.157770468C>T
Published as ACVR1(NM_001105.5):c.690G>A (p.E230=)
ISCN -
DB-ID ACVR1_000020 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) 0.96951 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACVR1 NM_001105.4 -/. - c.690G>A r.(?) p.(Glu230=)
ACVR1 NM_001111067.2 -/. - c.690G>A r.(?) p.(Glu230=)


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