Variant #0000545403 (NC_000011.9:g.67766704G>A, NM_030930.2:c.626C>T (UNC93B1))

Chromosome 11
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.67766704G>A
DNA change (hg38) g.67999234G>A
Published as UNC93B1(NM_030930.2):c.626C>T (p.P209L, p.(Pro209Leu))
ISCN -
DB-ID UNC93B1_000005 See all 3 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) 0.00386 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-01 09:51:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UNC93B1 NM_030930.2 -?/. - c.626C>T r.(?) p.(Pro209Leu)


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