Variant #0000509714 (NC_000002.11:g.158637039G>C, NM_001105.4:c.141C>G (ACVR1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.158637039G>C
DNA change (hg38) g.157780527G>C
Published as ACVR1(NM_001105.4):c.141C>G (p.(His47Gln)), ACVR1(NM_001105.5):c.141C>G (p.H47Q)
ISCN -
DB-ID ACVR1_000033 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) 0.00036 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 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     
ACVR1 NM_001105.4 -?/. - c.141C>G r.(?) p.(His47Gln)
ACVR1 NM_001111067.2 -?/. - c.141C>G r.(?) p.(His47Gln)


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