Variant #0000930615 (NC_000016.9:g.51175346C>A, NM_002968.2:c.787G>T (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.51175346C>A
DNA change (hg38) -
Published as SALL1(NM_001127892.1):c.496G>T (p.(Asp166Tyr)), SALL1(NM_002968.2):c.787G>T (p.D263Y), SALL1(NM_002968.3):c.787G>T (p.D263Y)
ISCN -
DB-ID SALL1_000034 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) 9.0E-5 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 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SALL1 NM_002968.2 -?/. - c.787G>T r.(?) p.(Asp263Tyr)


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