Variant #0000516248 (NC_000002.11:g.48010654C>G, NC_000002.11(NM_000179.2):c.260+22C>G (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48010654C>G
DNA change (hg38) g.47783515C>G
Published as MSH6(NM_000179.2):c.260+22C>G, MSH6(NM_000179.3):c.260+22C>G
ISCN -
DB-ID MSH6_000013 See all 28 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) 0.13624 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 -/. - c.260+22C>G r.(=) p.(=)
FBXO11 NM_001190274.1 -/. - c.*24603G>C r.(=) p.(=)


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