Variant #0000717506 (NC_000001.10:g.43888546C>T, NM_015284.3:c.2029C>T (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.43888546C>T
DNA change (hg38) -
Published as SZT2(NM_001365999.1):c.2029C>T (p.(Arg677Trp)), SZT2(NM_015284.4):c.2029C>T (p.R677W)
ISCN -
DB-ID HYI_000074 See all 2 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) 3.0E-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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SZT2 NM_015284.3 ?/. - c.2029C>T r.(?) p.(Arg677Trp)
HYI NM_031207.5 ?/. - c.*28435G>A r.(=) p.(=)


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