Variant #0000507568 (NC_000001.10:g.43905057C>G, NM_015284.3:c.6650C>G (SZT2))

Chromosome 1
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.43905057C>G
DNA change (hg38) g.43439386C>G
Published as SZT2(NM_015284.4):c.6650C>G (p.P2217R)
ISCN -
DB-ID HYI_000024
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) 1.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SZT2 NM_015284.3 ?/. - c.6650C>G r.(?) p.(Pro2217Arg)
HYI NM_031207.5 ?/. - c.*11924G>C r.(=) p.(=)


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