Variant #0000520872 (NC_000003.11:g.9979696C>T, NC_000003.11(NM_015513.4):c.369-3C>T (CRELD1))

Chromosome 3
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.9979696C>T
DNA change (hg38) g.9938012C>T
Published as CRELD1(NM_001077415.3):c.369-3C>T, CRELD1(NM_015513.4):c.369-3C>T
ISCN -
DB-ID IL17RC_000024 See all 3 reported entries
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) 0.00058 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRELD1 NM_015513.4 -?/. - c.369-3C>T r.spl? p.?
IL17RC NM_032732.5 -?/. - c.*4419C>T r.(=) p.(=)


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