Variant #0000347210 (NC_000017.10:g.66533655A>G, NM_017565.3:c.1589T>C (FAM20A))

Chromosome 17
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.66533655A>G
DNA change (hg38) g.68537514A>G
Published as -
ISCN -
DB-ID FAM20A_000007
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) 0.71316 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 -/. - c.*117051A>G r.(=) p.(=)
PRKAR1A NM_002734.4 -/. - c.*7065A>G r.(=) p.(=)
ARSG NM_014960.4 -/. - c.*117051A>G r.(=) p.(=)
FAM20A NM_017565.3 -/. - c.1589T>C r.(?) p.(Leu530Ser)
WIPI1 NM_017983.5 -/. - c.-80093T>C r.(?) p.(=)


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