Variant #0000969197 (NC_000017.10:g.66511643A>G, NM_017565.3:c.*21975T>C (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.66511643A>G
DNA change (hg38) -
Published as PRKAR1A(NM_002734.5):c.103A>G (p.I35V)
ISCN -
DB-ID FAM20A_000045
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) 0.00012 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 -?/. - c.*95039A>G r.(=) p.(=)
PRKAR1A NM_002734.4 -?/. - c.103A>G r.(?) p.(Ile35Val)
ARSG NM_014960.4 -?/. - c.*95039A>G r.(=) p.(=)
FAM20A NM_017565.3 -?/. - c.*21975T>C r.(=) p.(=)
WIPI1 NM_017983.5 -?/. - c.-58081T>C r.(?) p.(=)


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