Variant #0000911749 (NC_000002.11:g.48023227_48023229del, NC_000002.11(NM_000179.2):c.627+25_627+27del (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.48023227_48023229del
DNA change (hg38) -
Published as MSH6(NM_000179.2):c.627+25_627+27delGTT, MSH6(NM_000179.3):c.627+25_627+27delGTT
ISCN -
DB-ID MSH6_000128 See all 4 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_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.627+25_627+27del r.(=) p.(=)
FBXO11 NM_001190274.1 -?/. - c.*12031_*12033del r.(=) p.(=)


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