Variant #0000322338 (NC_000011.9:g.66611335G>A, NM_001040716.1:c.*5035C>T (PC))

Chromosome 11
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.66611335G>A
DNA change (hg38) g.66843864G>A
Published as RCE1(NM_001032279.1):c.-21+3G>A (p.(=))
ISCN -
DB-ID C11orf80_000005
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 2020-07-01 09:37:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PC NM_001040716.1 ?/. - c.*5035C>T r.(=) p.(=)
RCE1 NM_005133.2 ?/. - c.288+3G>A r.spl? p.?
LRFN4 NM_024036.4 ?/. - c.-13881G>A r.(?) p.(=)
C11orf80 NM_024650.3 ?/. - c.*630G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.