Variant #0000546909 (NC_000012.11:g.122693045G>A, NM_019887.5:c.603C>T (DIABLO))

Chromosome 12
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.122693045G>A
DNA change (hg38) g.122208498G>A
Published as DIABLO(NM_001278304.1):c.444C>T (p.S148=)
ISCN -
DB-ID B3GNT4_000002
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 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-03 11:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DIABLO NM_019887.5 -?/. - c.603C>T r.(?) p.(Ser201=)
B3GNT4 NM_030765.2 -?/. - c.*1110G>A r.(=) p.(=)


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