Variant #0000883337 (NC_000001.10:g.243468435C>T, NC_000001.10(NM_006642.3):c.740+356C>T (SDCCAG8))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.243468435C>T
DNA change (hg38) -
Published as SDCCAG8(NM_006642.5):c.740+356C>T
ISCN -
DB-ID SDCCAG8_000062 See all 8 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT3 NM_005465.4 +/. - c.*200116G>A r.(=) p.(=)
SDCCAG8 NM_006642.3 +/. - c.740+356C>T r.(=) p.(=)
AKT3 NM_181690.2 +/. - c.*183324G>A r.(=) p.(=)


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