Variant #0000658816 (NC_000021.8:g.33074560_33074563del, NM_020706.2:c.453_456del (SCAF4))

Chromosome 21
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.33074560_33074563del
DNA change (hg38) g.31702247_31702250del
Published as SCAF4(NM_020706.2):c.453_456delTGAA (p.N151Kfs*8)
ISCN -
DB-ID SCAF4_000019 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCAF4 NM_020706.2 ?/. - c.453_456del r.(?) p.(Asn151LysfsTer8)


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