Variant #0000330389 (NC_000005.9:g.60628591_60628605del, NM_020928.1:c.492_506del (ZSWIM6))

Chromosome 5
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.60628591_60628605del
DNA change (hg38) g.61332764_61332778del
Published as ZSWIM6(NM_020928.1):c.476_490del (p.(Thr167_Ala171del))
ISCN -
DB-ID ZSWIM6_000009
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZSWIM6 NM_020928.1 -?/. - c.492_506del r.(?) p.(Thr167_Ala171del)


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