Variant #0000865473 (NC_000017.10:g.66533733G>A, NM_017565.3:c.1511C>T (FAM20A))

Chromosome 17
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.66533733G>A
DNA change (hg38) -
Published as FAM20A(NM_001243746.1):c.1097C>T (p.(Thr366Ile))
ISCN -
DB-ID FAM20A_000039
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) 0.0015 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 2022-05-09 16:01:56 +02:00 (CEST)
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.*117129G>A r.(=) p.(=)
PRKAR1A NM_002734.4 -?/. - c.*7143G>A r.(=) p.(=)
ARSG NM_014960.4 -?/. - c.*117129G>A r.(=) p.(=)
FAM20A NM_017565.3 -?/. - c.1511C>T r.(?) p.(Thr504Ile)
WIPI1 NM_017983.5 -?/. - c.-80171C>T r.(?) p.(=)


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