Variant #0000799376 (NC_000001.10:g.43908298T>G, NC_000001.10(NM_015284.3):c.7980+9T>G (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.43908298T>G
DNA change (hg38) -
Published as SZT2(NM_001365999.1):c.8151+9T>G
ISCN -
DB-ID HYI_000083
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) 0.00018 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 2021-09-17 14:40:49 +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.7980+9T>G r.(=) p.(=)
HYI NM_031207.5 -?/. - c.*8683A>C r.(=) p.(=)


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