Variant #0000691820 (NC_000015.9:g.55722919A>T, NM_130810.3:c.1212T>A (DYX1C1))

Chromosome 15
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.55722919A>T
DNA change (hg38) -
Published as DNAAF4(NM_001033559.2):c.1106T>A (p.L369*)
ISCN -
DB-ID CCPG1_000009
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C15orf65 NM_001198784.1 ?/. - c.*12151A>T r.(=) p.(=)
CCPG1 NM_004748.4 ?/. - c.-22884T>A r.(?) p.(=)
PIGB NM_004855.4 ?/. - c.*75289A>T r.(=) p.(=)
DYX1C1 NM_130810.3 ?/. - c.1212T>A r.(?) p.(Ile404=)
DYX1C1-CCPG1 NR_037923.1 ?/. - n.1408+1776T>A r.(?) -


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