Variant #0000616067 (NC_000016.9:g.67183232G>C, NM_003789.3:c.*5320C>G (TRADD))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.67183232G>C
DNA change (hg38) g.67149329G>C
Published as B3GNT9(NM_033309.3):c.1157C>G (p.A386G)
ISCN -
DB-ID B3GNT9_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRADD NM_003789.3 ?/. - c.*5320C>G r.(=) p.(=)
C16orf70 NM_025187.3 ?/. - c.*2198G>C r.(=) p.(=)
B3GNT9 NM_033309.2 ?/. - c.1157C>G r.(?) p.(Ala386Gly)


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