Variant #0000722800 (NC_000010.10:g.28149778G>C, NC_000010.10(NM_018076.2):c.2800-3C>G (ARMC4))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.28149778G>C
DNA change (hg38) -
Published as ARMC4(NM_001290020.1):c.2800-3C>G, ODAD2(NM_001290020.2):c.2800-3C>G
ISCN -
DB-ID ARMC4_000026 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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     
ARMC4 NM_018076.2 +?/. - c.2800-3C>G r.spl? p.?


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