Variant #0000541742 (NC_000010.10:g.99258026G>A, NC_000010.10(NM_022362.4):c.112+4C>T (MMS19))

Chromosome 10
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.99258026G>A
DNA change (hg38) g.97498269G>A
Published as MMS19(NM_022362.4):c.112+4C>T (p.?)
ISCN -
DB-ID MMS19_000007
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) 0.01021 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-29 09:42:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMS19 NM_022362.4 -?/. - c.112+4C>T r.spl? p.?
UBTD1 NM_024954.3 -?/. - c.-935G>A r.(?) p.(=)


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