Variant #0000973975 (NC_000001.10:g.43881759G>A, NM_015284.3:c.759G>A (SZT2))

Chromosome 1
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.43881759G>A
DNA change (hg38) -
Published as SZT2(NM_001365999.1):c.759G>A (p.(Ser253=)), SZT2(NM_015284.3):c.759G>A (p.S253=)
ISCN -
DB-ID SZT2_000034 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) 0.00186 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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SZT2 NM_015284.3 -?/. - c.759G>A r.(?) p.(Ser253=)
HYI NM_031207.5 -?/. - c.*35222C>T r.(=) p.(=)


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