Variant #0000966639 (NC_000011.9:g.94224075A>G, NM_005591.3:c.77T>C (MRE11A))

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.94224075A>G
DNA change (hg38) -
Published as MRE11A(NM_005590.3):c.77T>C (p.M26T), MRE11A(NM_005591.3):c.77T>C (p.M26T)
ISCN -
DB-ID MRE11A_000402 See all 3 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) 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRE11A NM_005591.3 ?/. - c.77T>C r.(?) p.(Met26Thr)
ANKRD49 NM_017704.2 ?/. - c.-3217A>G r.(?) p.(=)


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