Variant #0000854089 (NC_000015.9:g.55727237T>G, NM_130810.3:c.913A>C (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.55727237T>G
DNA change (hg38) -
Published as DNAAF4(NM_130810.4):c.913A>C (p.N305H)
ISCN -
DB-ID CCPG1_000014
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 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.*16469T>G r.(=) p.(=)
CCPG1 NM_004748.4 ?/. - c.-27202A>C r.(?) p.(=)
PIGB NM_004855.4 ?/. - c.*79607T>G r.(=) p.(=)
DYX1C1 NM_130810.3 ?/. - c.913A>C r.(?) p.(Asn305His)
DYX1C1-CCPG1 NR_037923.1 ?/. - n.1168A>C r.(?) -


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