Variant #0000565398 (NC_000018.9:g.72997855_72997859del, NM_005786.5:c.358_362del (TSHZ1))

Chromosome 18
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.72997855_72997859del
DNA change (hg38) g.75285900_75285904del
Published as TSHZ1(NM_005786.5):c.358_362del (p.(Val120Hisfs*53))
ISCN -
DB-ID TSHZ1_000026
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) 0.00061 View details
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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSHZ1 NM_005786.5 -?/. - c.358_362del r.(?) p.(Val120HisfsTer53)


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