Variant #0000256509 (NC_000015.9:g.55652389A>C, NM_130810.3:c.*70479T>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.55652389A>C
DNA change (hg38) g.55360191A>C
Published as CCPG1(NM_004748.4):c.1582T>G (p.S528A)
ISCN -
DB-ID CCPG1_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-06 15:03:08 +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.-48578A>C r.(?) p.(=)
CCPG1 NM_004748.4 ?/. - c.1582T>G r.(?) p.(Ser528Ala)
PIGB NM_004855.4 ?/. - c.*4759A>C r.(=) p.(=)
DYX1C1 NM_130810.3 ?/. - c.*70479T>G r.(=) p.(=)
DYX1C1-CCPG1 NR_037923.1 ?/. - n.2999T>G r.(?) -


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