Variant #0000861984 (NC_000010.10:g.75670996G>A, NM_001001791.2:c.*447C>T (C10orf55))

Chromosome 10
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.75670996G>A
DNA change (hg38) -
Published as PLAU(NM_002658.3):c.-32+20G>A
ISCN -
DB-ID C10orf55_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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +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     
C10orf55 NM_001001791.2 -?/. - c.*447C>T r.(=) p.(=)
PLAU NM_002658.3 -?/. - c.-32+20G>A r.(=) p.(=)


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