Variant #0000854090 (NC_000015.9:g.55759342C>T, NM_130810.3:c.423G>A (DYX1C1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55759342C>T
DNA change (hg38) -
Published as DNAAF4(NM_130810.3):c.423G>A (p.R141=)
ISCN -
DB-ID CCPG1_000015
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 2022-05-09 15:47:41 +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.*48574C>T r.(=) p.(=)
CCPG1 NM_004748.4 -?/. - c.-59307G>A r.(?) p.(=)
PIGB NM_004855.4 -?/. - c.*111712C>T r.(=) p.(=)
DYX1C1 NM_130810.3 -?/. - c.423G>A r.(?) p.(Arg141=)
DYX1C1-CCPG1 NR_037923.1 -?/. - n.678G>A r.(?) -


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