Variant #0000977671 (NC_000007.13:g.295970T>A, NM_020223.3:c.1228T>A (FAM20C))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.295970T>A
DNA change (hg38) -
Published as FAM20C(NM_020223.3):c.1228T>A (p.(Ser410Thr)), FAM20C(NM_020223.4):c.1228T>A (p.S410T)
ISCN -
DB-ID FAM20C_000050 See all 4 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) 0.00492 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM20C NM_020223.3 -/. - c.1228T>A r.(?) p.(Ser410Thr)


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