Variant #0000291971 (NC_000011.9:g.94224032G>A, NM_005591.3:c.120C>T (MRE11A))

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.94224032G>A
DNA change (hg38) g.94490866G>A
Published as MRE11(NM_005591.3):c.120C>T (p.L40=), MRE11(NM_005591.4):c.120C>T (p.L40=), MRE11A(NM_001330347.1):c.120C>T (p.L40=)
ISCN -
DB-ID MRE11A_000023 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) 0.00055 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRE11A NM_005591.3 -?/. - c.120C>T r.(?) p.(Leu40=)
ANKRD49 NM_017704.2 -?/. - c.-3260G>A r.(?) p.(=)


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