Variant #0000614284 (NC_000012.11:g.52310026C>T, NC_000012.11(NM_000020.2):c.1246+9C>T (ACVRL1))

Chromosome 12
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.52310026C>T
DNA change (hg38) g.51916242C>T
Published as ACVRL1(NM_000020.2):c.1246+9C>T, ACVRL1(NM_000020.3):c.1246+9C>T
ISCN -
DB-ID ACVRL1_000061 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) 0.00228 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
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     
ACVRL1 NM_000020.2 -/. - c.1246+9C>T r.(=) p.(=)


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