Variant #0000657499 (NC_000014.8:g.77796707G>T, NC_000014.8(NM_145870.2):c.524+5G>T (GSTZ1))

Chromosome 14
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.77796707G>T
DNA change (hg38) g.77330364G>T
Published as GSTZ1(NM_001312660.1):c.359+5G>T
ISCN -
DB-ID GSTZ1_000007
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) 2.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-05 16:20:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GSTZ1 NM_145870.2 -?/. - c.524+5G>T r.spl? p.?
TMED8 NM_213601.1 -?/. - c.*11407C>A r.(=) p.(=)


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