Variant #0000322056 (NC_000011.9:g.8642123C>A, NM_000990.4:c.-62238C>A (RPL27A))

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.8642123C>A
DNA change (hg38) g.8620576C>A
Published as TRIM66(NM_001388022.1):c.3546-4G>T (p.?)
ISCN -
DB-ID TRIM66_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) 0.00023 View details
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 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL27A NM_000990.4 ?/. - c.-62238C>A r.(?) p.(=)
TRIM66 NM_014818.1 ?/. - c.3018-4G>T r.spl? p.?


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