Variant #0000507557 (NC_000001.10:g.43896743C>T, NM_015284.3:c.4727C>T (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.43896743C>T
DNA change (hg38) g.43431072C>T
Published as SZT2(NM_001365999.1):c.4898C>T (p.S1633L), SZT2(NM_015284.4):c.4727C>T (p.S1576L)
ISCN -
DB-ID SZT2_000008 See all 4 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) 0.00188 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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.4727C>T r.(?) p.(Ser1576Leu)
HYI NM_031207.5 -?/. - c.*20238G>A r.(=) p.(=)


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