Variant #0000340643 (NC_000020.10:g.50407966C>T, NM_020436.3:c.1056G>A (SALL4))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50407966C>T
DNA change (hg38) g.51791427C>T
Published as SALL4(NM_020436.3):c.1056G>A (p.A352=), SALL4(NM_020436.5):c.1056G>A (p.A352=)
ISCN -
DB-ID SALL4_000019 See all 3 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) 0.24689 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
SALL4 NM_020436.3 -/. - c.1056G>A r.(?) p.(Ala352=)


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