Variant #0001026466 (NC_000015.9:g.55742479A>C, NM_130810.3:c.724T>G (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.55742479A>C
DNA change (hg38) -
Published as DNAAF4(NM_130810.4):c.724T>G (p.F242V)
ISCN -
DB-ID CCPG1_000024
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +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.*31711A>C r.(=) p.(=)
CCPG1 NM_004748.4 ?/. - c.-42444T>G r.(?) p.(=)
PIGB NM_004855.4 ?/. - c.*94849A>C r.(=) p.(=)
DYX1C1 NM_130810.3 ?/. - c.724T>G r.(?) p.(Phe242Val)
DYX1C1-CCPG1 NR_037923.1 ?/. - n.979T>G r.(?) -


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