Variant #0000555273 (NC_000015.9:g.71146260G>T, NM_018357.2:c.168C>A (LARP6))

Chromosome 15
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.71146260G>T
DNA change (hg38) g.70853921G>T
Published as LARP6(NM_018357.3):c.168C>A (p.S56R)
ISCN -
DB-ID LARP6_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
LRRC49 NM_017691.3 ?/. - c.-38974G>T r.(?) p.(=)
LARP6 NM_018357.2 ?/. - c.168C>A r.(?) p.(Ser56Arg)
THAP10 NM_020147.3 ?/. - c.*28533C>A r.(=) p.(=)


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