Variant #0000565248 (NC_000018.9:g.675344G>A, NM_001071.2:c.*2347G>A (TYMS))

Chromosome 18
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.675344G>A
DNA change (hg38) g.675344G>A
Published as ENOSF1(NM_017512.7):c.1207C>T (p.R403W)
ISCN -
DB-ID ENOSF1_000002
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) 0.00025 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     
C18orf56 NM_001012716.2 ?/. - c.-17097C>T r.(?) p.(=)
TYMS NM_001071.2 ?/. - c.*2347G>A r.(=) p.(=)
ENOSF1 NM_017512.5 ?/. - c.1207C>T r.(?) p.(Arg403Trp)


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