Variant #0000965678 (NC_000010.10:g.16553103C>A, NM_001010908.1:c.*3424G>T (C1QL3))

Chromosome 10
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.16553103C>A
DNA change (hg38) -
Published as PTER(NM_001001484.3):c.898C>A (p.H300N)
ISCN -
DB-ID C1QL3_000003
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) 2.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1QL3 NM_001010908.1 ?/. - c.*3424G>T r.(=) p.(=)
PTER NM_030664.4 ?/. - c.898C>A r.(?) p.(His300Asn)


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