Variant #0000688690 (NC_000002.11:g.232156105A>G, NM_025139.4:c.1666A>G (ARMC9))

Chromosome 2
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.232156105A>G
DNA change (hg38) -
Published as ARMC9(NM_001291656.1):c.1666A>G (p.N556D)
ISCN -
DB-ID ARMC9_000025
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) 6.0E-5 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 2020-09-15 15:50:26 +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.1666A>G r.(?) p.(Asn556Asp)
ARMC9 NM_025139.4 ?/. - c.1666A>G r.(?) p.(Asn556Asp)


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