Variant #0000717513 (NC_000001.10:g.43908593G>A, NM_015284.3:c.8084G>A (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.43908593G>A
DNA change (hg38) -
Published as SZT2(NM_001365999.1):c.8255G>A (p.R2752H), SZT2(NM_015284.4):c.8084G>A (p.R2695H)
ISCN -
DB-ID SZT2_000019 See all 3 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) 0.0008 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.8084G>A r.(?) p.(Arg2695His)
HYI NM_031207.5 ?/. - c.*8388C>T r.(=) p.(=)


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