Variant #0000681645 (NC_000020.10:g.50401133C>T, NM_020436.3:c.2833G>A (SALL4))

Chromosome 20
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.50401133C>T
DNA change (hg38) -
Published as SALL4(NM_001318031.2):c.1522G>A (p.D508N), SALL4(NM_020436.3):c.2833G>A (p.(Asp945Asn))
ISCN -
DB-ID SALL4_000004 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) 0 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +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     
SALL4 NM_020436.3 ?/. - c.2833G>A r.(?) p.(Asp945Asn)


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