Variant #0000307851 (NC_000001.10:g.243456443C>A, NM_006642.3:c.597C>A (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.243456443C>A
DNA change (hg38) g.243293141C>A
Published as SDCCAG8(NM_001350248.1):c.597C>A (p.G199=), SDCCAG8(NM_001350248.2):c.597C>A (p.G199=)
ISCN -
DB-ID SDCCAG8_000012 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) 0.00019 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +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.*212108G>T r.(=) p.(=)
SDCCAG8 NM_006642.3 -?/. - c.597C>A r.(?) p.(Gly199=)
AKT3 NM_181690.2 -?/. - c.*195316G>T r.(=) p.(=)


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