Variant #0001042136 (NC_000017.10:g.66538153C>T, NM_017565.3:c.1082G>A (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.66538153C>T
DNA change (hg38) -
Published as FAM20A(NM_017565.4):c.1082G>A (p.(Arg361His))
ISCN -
DB-ID FAM20A_000062
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) 5.0E-5 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 2025-05-05 21:14:00 +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     
PRKAR1A NM_002734.4 -?/. - c.*11563C>T r.(=) p.(=)
FAM20A NM_017565.3 -?/. - c.1082G>A r.(?) p.(Arg361His)


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