Variant #0000572404 (NC_000022.10:g.50969245del, NM_001257988.1:c.-955del (TYMP))

Chromosome 22
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.50969245del
DNA change (hg38) g.50530816del
Published as ODF3B(NM_001014440.3):c.580delG (p.(Val194SerfsTer55))
ISCN -
DB-ID NCAPH2_000021
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-17 16:15:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ODF3B NM_001014440.3 ?/. - c.580del r.(?) p.(Val194SerfsTer55)
TYMP NM_001257988.1 ?/. - c.-955del r.(?) p.(=)
SCO2 NM_005138.2 ?/. - c.-5355del r.(?) p.(=)
NCAPH2 NM_152299.3 ?/. - c.*7441del r.(?) p.(=)


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