Variant #0000570013 (NC_000020.10:g.55101017C>T, NM_001012971.3:c.407C>T (FAM209A))

Chromosome 20
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.55101017C>T
DNA change (hg38) g.56525961C>T
Published as FAM209A(NM_001012971.3):c.407C>T (p.A136V)
ISCN -
DB-ID FAM209A_000004
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) 0.00013 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM209A NM_001012971.3 -?/. - c.407C>T r.(?) p.(Ala136Val)
RTFDC1 NM_016407.3 -?/. - c.*7696C>T r.(=) p.(=)
GCNT7 NM_080615.1 -?/. - c.-742G>A r.(?) p.(=)


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