Variant #0000805384 (NC_000011.9:g.71817218G>C, NM_001145309.3:c.320G>C (LRTOMT))

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.71817218G>C
DNA change (hg38) -
Published as LRTOMT(NM_001145309.3):c.320G>C (p.S107T)
ISCN -
DB-ID LAMTOR1_000013
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
LRTOMT NM_001145309.3 ?/. - c.320G>C r.(?) p.(Ser107Thr)
NUMA1 NM_006185.2 ?/. - c.-25817C>G r.(?) p.(=)
ANAPC15 NM_014042.2 ?/. - c.*3709C>G r.(=) p.(=)
LAMTOR1 NM_017907.2 ?/. - c.-2948C>G r.(?) p.(=)


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