Variant #0000507613 (NC_000001.10:g.45272150C>A, NM_001136537.1:c.-2343C>A (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.45272150C>A
DNA change (hg38) g.44806478C>A
Published as TCTEX1D4(NM_001013632.2):c.191G>T (p.(Arg64Leu))
ISCN -
DB-ID BTBD19_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) 0.00021 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
TCTEX1D4 NM_001013632.2 ?/. - c.191G>T r.(?) p.(Arg64Leu)
BTBD19 NM_001136537.1 ?/. - c.-2343C>A r.(?) p.(=)
PLK3 NM_004073.2 ?/. - c.*800C>A r.(=) p.(=)


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