Variant #0000883338 (NC_000001.10:g.243471294C>T, NM_006642.3:c.744C>T (SDCCAG8))

Chromosome 1
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.243471294C>T
DNA change (hg38) -
Published as SDCCAG8(NM_001350248.2):c.840C>T (p.N280=), SDCCAG8(NM_006642.4):c.744C>T (p.N248=)
ISCN -
DB-ID SDCCAG8_000014 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) 0.00017 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +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     
AKT3 NM_005465.4 -?/. - c.*197257G>A r.(=) p.(=)
SDCCAG8 NM_006642.3 -?/. - c.744C>T r.(?) p.(Asn248=)
AKT3 NM_181690.2 -?/. - c.*180465G>A r.(=) p.(=)


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