Variant #0000295705 (NC_000001.10:g.243542017C>T, NC_000001.10(NM_006642.3):c.1474-6C>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.243542017C>T
DNA change (hg38) g.243378715C>T
Published as SDCCAG8(NM_001350251.2):c.571-6C>T, SDCCAG8(NM_006642.4):c.1474-6C>T
ISCN -
DB-ID SDCCAG8_000024 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) 0.00072 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKT3 NM_005465.4 -?/. - c.*126534G>A r.(=) p.(=)
SDCCAG8 NM_006642.3 -?/. - c.1474-6C>T r.(=) p.(=)
AKT3 NM_181690.2 -?/. - c.*109742G>A r.(=) p.(=)


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