Variant #0000546130 (NC_000011.9:g.95564259A>G, NM_016156.5:c.*4195T>C (MTMR2))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.95564259A>G
DNA change (hg38) g.95831095A>G
Published as CEP57(NM_001243776.2):c.1315A>G (p.R439G)
ISCN -
DB-ID CEP57_000016
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) 0.29718 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP57 NM_014679.4 -/. - c.1342A>G r.(?) p.(Arg448Gly)
MTMR2 NM_016156.5 -/. - c.*4195T>C r.(=) p.(=)


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