Variant #0000886032 (NC_000003.11:g.9972602G>A, NM_015513.4:c.-3521G>A (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.9972602G>A
DNA change (hg38) -
Published as IL17RC(NM_153461.3):c.1575G>A (p.A525=), IL17RC(NM_153461.4):c.1575G>A (p.A525=)
ISCN -
DB-ID IL17RC_000048 See all 2 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) 0.00113 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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     
CRELD1 NM_015513.4 -?/. - c.-3521G>A r.(?) p.(=)
IL17RC NM_032732.5 -?/. - c.1317G>A r.(?) p.(Ala439=)


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