Variant #0000539814 (NC_000010.10:g.28233185C>T, NM_018076.2:c.1709G>A (ARMC4))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.28233185C>T
DNA change (hg38) g.27944256C>T
Published as ARMC4(NM_018076.2):c.1709G>A (p.(Arg570Gln)), ODAD2(NM_001290020.2):c.1709G>A (p.R570Q)
ISCN -
DB-ID ARMC4_000005 See all 3 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) 0.00048 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 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     
ARMC4 NM_018076.2 ?/. - c.1709G>A r.(?) p.(Arg570Gln)


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