Variant #0000992932 (NC_000002.11:g.48132740_48132741insAGCTGCTGCTGGGGC, NM_000179.2:c.*98741_*98742insAGCTGCTGCTGGGGC (MSH6))

Chromosome 2
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.48132740_48132741insAGCTGCTGCTGGGGC
DNA change (hg38) -
Published as FBXO11(NM_001190274.1):c.133_134insTGCCCCAGCAGCAGC (p.(Gln44_Pro45insLeuProGlnGlnGln))
ISCN -
DB-ID MSH6_011144
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
MSH6 NM_000179.2 ?/. - c.*98741_*98742insAGCTGCTGCTGGGGC r.(=) p.(=)
FBXO11 NM_001190274.1 ?/. - c.133_134insTGCCCCAGCAGCAGC r.(?) p.(Gln44_Pro45insLeuProGlnGlnGln)


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