Variant #0000305902 (NC_000001.10:g.45269669C>T, NM_001136537.1:c.-4824C>T (BTBD19))

Chromosome 1
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.45269669C>T
DNA change (hg38) g.44803997C>T
Published as PLK3(NM_004073.4):c.1231C>T (p.R411C)
ISCN -
DB-ID PLK3_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) 7.0E-5 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 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     
TCTEX1D4 NM_001013632.2 ?/. - c.*2006G>A r.(=) p.(=)
BTBD19 NM_001136537.1 ?/. - c.-4824C>T r.(?) p.(=)
PLK3 NM_004073.2 ?/. - c.1231C>T r.(?) p.(Arg411Cys)


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