Variant #0000991316 (NC_000001.10:g.45272455C>T, NM_001136537.1:c.-2038C>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.45272455C>T
DNA change (hg38) -
Published as TCTEX1D4(NM_001013632.2):c.-8+1G>A (p.?)
ISCN -
DB-ID BTBD19_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCTEX1D4 NM_001013632.2 ?/. - c.-8+1G>A r.spl? p.?
BTBD19 NM_001136537.1 ?/. - c.-2038C>T r.(?) p.(=)
PLK3 NM_004073.2 ?/. - c.*1105C>T r.(=) p.(=)


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