Variant #0000725756 (NC_000016.9:g.31477780G>A, NM_024742.2:c.*1258G>A (ARMC5))

Chromosome 16
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.31477780G>A
DNA change (hg38) -
Published as ARMC5(NM_001105247.1):c.2378G>A (p.(Arg793Gln)), ARMC5(NM_001301820.1):c.2474G>A (p.R825Q)
ISCN -
DB-ID ARMC5_000021 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) 0.0002 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARMC5 NM_024742.2 ?/. - c.*1258G>A r.(=) p.(=)


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