Variant #0000545638 (NC_000011.9:g.71717267A>G, NM_001145309.3:c.-75207A>G (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.71717267A>G
DNA change (hg38) g.72006221A>G
Published as NUMA1(NM_001286561.1):c.5464T>C (p.Y1822H), NUMA1(NM_006185.2):c.5506T>C (p.(Tyr1836His))
ISCN -
DB-ID NUMA1_000001 See all 2 reported entries
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) 0.00543 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +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.-75207A>G r.(?) p.(=)
NUMA1 NM_006185.2 -?/. - c.5506T>C r.(?) p.(Tyr1836His)
IL18BP NM_173042.2 -?/. - c.*4360A>G r.(=) p.(=)


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