Variant #0000538945 (NC_000010.10:g.103717507_103717508dup, NC_000010.10(NM_024541.2):c.1496-6_1496-5dup (C10orf76))

Chromosome 10
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.103717507_103717508dup
DNA change (hg38) g.101957750_101957751dup
Published as ARMH3(NM_024541.3):c.1496-6_1496-5dupTT
ISCN -
DB-ID C10orf76_000002
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
C10orf76 NM_024541.2 -?/. - c.1496-6_1496-5dup r.spl? p.?


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