Variant #0000329225 (NC_000003.11:g.9975039C>G, NM_015513.4:c.-1084C>G (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.9975039C>G
DNA change (hg38) g.9933355C>G
Published as IL17RC(NM_001203263.1):c.1886C>G (p.(Ala629Gly))
ISCN -
DB-ID IL17RC_000006
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +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.-1084C>G r.(?) p.(=)
IL17RC NM_032732.5 ?/. - c.1880C>G r.(?) p.(Ala627Gly)


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