Variant #0000313869 (NC_000005.9:g.60628556_60628561del, NM_020928.1:c.457_462del (ZSWIM6))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.60628556_60628561del
DNA change (hg38) g.61332729_61332734del
Published as ZSWIM6(NM_020928.1):c.442_447del (p.(Gly150_Gly151del)), ZSWIM6(NM_020928.2):c.457_462delGGCGGC (p.G153_G154del)
ISCN -
DB-ID ZSWIM6_000007 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZSWIM6 NM_020928.1 ?/. - c.457_462del r.(?) p.(Gly153_Gly154del)


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