Variant #0000885014 (NC_000002.11:g.232146762C>T, NC_000002.11(NM_025139.4):c.1552-10C>T (ARMC9))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.232146762C>T
DNA change (hg38) -
Published as ARMC9(NM_001271466.3):c.1552-10C>T, ARMC9(NM_025139.6):c.1552-10C>T
ISCN -
DB-ID ARMC9_000007 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) 0.0015 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 2022-11-01 13:01:21 +01:00 (CET)
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.1552-10C>T r.(=) p.(=)
ARMC9 NM_025139.4 -?/. - c.1552-10C>T r.(=) p.(=)


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