Variant #0000849788 (NC_000002.11:g.232087474A>G, NM_025139.4:c.538= (ARMC9))

Chromosome 2
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.232087474A>G
DNA change (hg38) -
Published as ARMC9(NM_025139.6):c.538_539delATinsGT (p.I180V)
ISCN -
DB-ID ARMC9_000035
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) 0.99992 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARMC9 NM_001352754.1 -/. - c.538= r.(=) p.(Glu180=)
ARMC9 NM_025139.4 -/. - c.538= r.(=) p.(Glu180=)


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