Variant #0000895820 (NC_000022.10:g.50964699_50964701del, NM_001257988.1:c.1138_1140del (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.50964699_50964701del
DNA change (hg38) -
Published as TYMP(NM_001113755.2):c.1138_1140del (p.(Glu380del))
ISCN -
DB-ID NCAPH2_000044
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 2022-11-01 13:41:49 +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     
ODF3B NM_001014440.3 ?/. - c.*4213_*4215del r.(=) p.(=)
TYMP NM_001257988.1 ?/. - c.1138_1140del r.(?) p.(Glu380del)
SCO2 NM_005138.2 ?/. - c.-809_-807del r.(?) p.(=)
NCAPH2 NM_152299.3 ?/. - c.*2895_*2897del r.(=) p.(=)


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