Variant #0001055890 (NC_000017.10:g.18217944G>A, NM_004618.3:c.149C>T (TOP3A))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.18217944G>A
DNA change (hg38) -
Published as TOP3A(NM_004618.5):c.149C>T (p.(Ala50Val))
ISCN -
DB-ID SHMT1_000010
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHMT1 NM_004169.3 ?/. - c.*14120C>T r.(=) p.(=)
TOP3A NM_004618.3 ?/. - c.149C>T r.(?) p.(Ala50Val)
SMCR8 NM_144775.2 ?/. - c.-1160G>A r.(?) p.(=)


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