Variant #0000849965 (NC_000002.11:g.48033984_48033987dup, NM_000179.2:c.4068_4071dup (MSH6))

Chromosome 2
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.48033984_48033987dup
DNA change (hg38) -
Published as MSH6(NM_000179.2):c.4068_4071dup (p.(Lys1358Aspfs*2)), MSH6(NM_000179.2):c.4068_4071dupGATT (p.K1358Dfs*2), MSH6(NM_000179.3):c.4068_4071dupGATT ...)
ISCN -
DB-ID MSH6_000119 See all 16 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 -?/. - c.4068_4071dup r.(?) p.(Lys1358AspfsTer2)
FBXO11 NM_001190274.1 -?/. - c.*1272_*1275dup r.(=) p.(=)


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