Variant #0000574279 (NC_000023.10:g.152853846T>C, NM_152274.3:c.724A>G (FAM58A))

Chromosome X
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.152853846T>C
DNA change (hg38) g.153588388T>C
Published as CCNQ(NM_152274.4):c.724A>G (p.T242A), CCNQ(NM_152274.5):c.718A>G (p.(Thr240Ala)), CCNQ(NM_152274.5):c.724A>G (p.T242A)
ISCN -
DB-ID FAM58A_000010 See all 3 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) 0.00187 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.724A>G r.(?) p.(Thr242Ala)


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