Variant #0000328623 (NC_000020.10:g.62707238_62707242del, NM_001007125.1:c.*7499_*7503del (C20orf201))

Chromosome 20
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.62707238_62707242del
DNA change (hg38) g.64075885_64075889del
Published as RGS19(NM_001039467.1):c.152+639_152+643del (p.(=))
ISCN -
DB-ID RGS19_000001
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     
C20orf201 NM_001007125.1 ?/. - c.*7499_*7503del r.(=) p.(=)
RGS19 NM_005873.2 ?/. - c.152+639_152+643del r.(=) p.(=)
OPRL1 NM_182647.2 ?/. - c.-4652_-4648del r.(?) p.(=)
TCEA2 NM_198723.1 ?/. - c.*3705_*3709del r.(=) p.(=)


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