Variant #0000892156 (NC_000015.9:g.55727162G>A, NM_130810.3:c.988C>T (DYX1C1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55727162G>A
DNA change (hg38) -
Published as DNAAF4(NM_130810.4):c.988C>T (p.R330W)
ISCN -
DB-ID CCPG1_000017
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) 2.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.*16394G>A r.(=) p.(=)
CCPG1 NM_004748.4 +?/. - c.-27127C>T r.(?) p.(=)
PIGB NM_004855.4 +?/. - c.*79532G>A r.(=) p.(=)
DYX1C1 NM_130810.3 +?/. - c.988C>T r.(?) p.(Arg330Trp)
DYX1C1-CCPG1 NR_037923.1 +?/. - n.1243C>T r.(?) -


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