Variant #0000574283 (NC_000023.10:g.152860096C>T, NM_152274.3:c.338G>A (FAM58A))

Chromosome X
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.152860096C>T
DNA change (hg38) g.153594638C>T
Published as CCNQ(NM_152274.5):c.332G>A (p.(Arg111His)), FAM58A(NM_152274.4):c.338G>A (p.R113H)
ISCN -
DB-ID FAM58A_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) 0.00223 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM58A NM_152274.3 ?/. - c.338G>A r.(?) p.(Arg113His)


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