Variant #0000558404 (NC_000016.9:g.51175677_51175685del, NM_002968.2:c.469_477del (SALL1))

Chromosome 16
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.51175677_51175685del
DNA change (hg38) g.51141766_51141774del
Published as SALL1(NM_001127892.1):c.178_186del (p.(Ser60_Ser62del)), SALL1(NM_001127892.2):c.178_186delAGCAGCAGC (p.S60_S62del), SALL1(NM_002968.2):c.469_477de...
ISCN -
DB-ID SALL1_000041 See all 4 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SALL1 NM_002968.2 -?/. - c.469_477del r.(?) p.(Ser157_Ser159del)


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