Variant #0000554820 (NC_000015.9:g.55759223A>C, NM_130810.3:c.542T>G (DYX1C1))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55759223A>C
DNA change (hg38) g.55467025A>C
Published as DNAAF4(NM_130810.4):c.542T>G (p.L181*)
ISCN -
DB-ID CCPG1_000005
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C15orf65 NM_001198784.1 +/. - c.*48455A>C r.(=) p.(=)
CCPG1 NM_004748.4 +/. - c.-59188T>G r.(?) p.(=)
PIGB NM_004855.4 +/. - c.*111593A>C r.(=) p.(=)
DYX1C1 NM_130810.3 +/. - c.542T>G r.(?) p.(Leu181Ter)
DYX1C1-CCPG1 NR_037923.1 +/. - n.797T>G r.(?) -


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