Variant #0000994805 (NC_000005.9:g.149751653C>T, NM_001135243.1:c.724C>T (TCOF1))

Chromosome 5
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.149751653C>T
DNA change (hg38) -
Published as TCOF1(NM_001008657.2):c.724C>T (p.(Pro242Ser)), TCOF1(NM_001135243.2):c.724C>T (p.P242S)
ISCN -
DB-ID TCOF1_000006 See all 2 reported entries
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) 8.0E-5 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 2024-08-28 13:16:32 +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     
TCOF1 NM_001135243.1 -?/. - c.724C>T r.(?) p.(Pro242Ser)


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