Variant #0000691210 (NC_000011.9:g.8662112G>T, NM_000990.4:c.-42249G>T (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.8662112G>T
DNA change (hg38) -
Published as TRIM66(NM_014818.1):c.1375C>A (p.P459T)
ISCN -
DB-ID RPL27A_000003
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL27A NM_000990.4 -?/. - c.-42249G>T r.(?) p.(=)
TRIM66 NM_014818.1 -?/. - c.1375C>A r.(?) p.(Pro459Thr)


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