Variant #0000979933 (NC_000011.9:g.8640450C>G, NM_000990.4:c.-63911C>G (RPL27A))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.8640450C>G
DNA change (hg38) -
Published as TRIM66(NM_001388022.1):c.3966G>C (p.(Glu1322Asp))
ISCN -
DB-ID RPL27A_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) 0.00558 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL27A NM_000990.4 -?/. - c.-63911C>G r.(?) p.(=)
TRIM66 NM_014818.1 -?/. - c.3438G>C r.(?) p.(Glu1146Asp)


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