Variant #0000886699 (NC_000005.9:g.149751756_149751773del, NM_001135243.1:c.827_844del (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.149751756_149751773del
DNA change (hg38) -
Published as TCOF1(NM_001008657.2):c.817_834del (p.(Gly276_Glu281del)), TCOF1(NM_001135243.1):c.827_844delGATCTGAAAGTGAGGAGG (p.G276_E281del), TCOF1(NM_0011352...)
ISCN -
DB-ID TCOF1_000075 See all 3 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +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     
TCOF1 NM_001135243.1 -?/. - c.827_844del r.(?) p.(Gly276_Glu281del)


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