Variant #0000998627 (NC_000010.10:g.99215803T>C, NM_022362.4:c.*2646A>G (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.99215803T>C
DNA change (hg38) -
Published as ZDHHC16(NM_198046.1):c.1019+2T>C (p.?)
ISCN -
DB-ID MMS19_000010 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) 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 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMS19 NM_022362.4 ?/. - c.*2646A>G r.(=) p.(=)
ZDHHC16 NM_032327.2 ?/. - c.1019+2T>C r.spl? p.?
ZDHHC16 NM_198046.3 ?/. - c.1019+2T>C r.spl? p.?


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