Variant #0000805481 (NC_000011.9:g.95568531A>G, NM_016156.5:c.1855T>C (MTMR2))

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.95568531A>G
DNA change (hg38) -
Published as MTMR2(NM_001243571.2):c.1639T>C (p.S547P), MTMR2(NM_016156.5):c.1855T>C (p.S619P)
ISCN -
DB-ID CEP57_000019 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) 0.00285 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
CEP57 NM_014679.4 -?/. - c.*4111A>G r.(=) p.(=)
MTMR2 NM_016156.5 -?/. - c.1855T>C r.(?) p.(Ser619Pro)


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