Variant #0000608916 (NC_000003.11:g.9974652G>T, NM_015513.4:c.-1471G>T (CRELD1))

Chromosome 3
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.9974652G>T
DNA change (hg38) g.9932968G>T
Published as IL17RC(NM_153461.3):c.1751G>T (p.R584L)
ISCN -
DB-ID IL17RC_000029
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) 0.0001 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRELD1 NM_015513.4 ?/. - c.-1471G>T r.(?) p.(=)
IL17RC NM_032732.5 ?/. - c.1493G>T r.(?) p.(Arg498Leu)


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