Variant #0000613688 (NC_000011.9:g.71725284G>C, NM_001145309.3:c.-67190G>C (LRTOMT))

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.71725284G>C
DNA change (hg38) g.72014238G>C
Published as NUMA1(NM_001286561.1):c.3265C>G (p.Q1089E)
ISCN -
DB-ID NUMA1_000012
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) 0.0009 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 2019-12-04 15:24:38 +01:00 (CET)
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     
LRTOMT NM_001145309.3 -?/. - c.-67190G>C r.(?) p.(=)
NUMA1 NM_006185.2 -?/. - c.3265C>G r.(?) p.(Gln1089Glu)


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