Variant #0000804664 (NC_000010.10:g.99219980G>A, NM_022362.4:c.2479C>T (MMS19))

Chromosome 10
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.99219980G>A
DNA change (hg38) -
Published as MMS19(NM_001351356.1):c.2596C>T (p.L866F), MMS19(NM_022362.4):c.2479C>T (p.(Leu827Phe))
ISCN -
DB-ID MMS19_000008 See all 2 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) 0.00014 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMS19 NM_022362.4 ?/. - c.2479C>T r.(?) p.(Leu827Phe)
ZDHHC16 NM_032327.2 ?/. - c.*3332G>A r.(=) p.(=)


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