Variant #0000854575 (NC_000016.9:g.58035491G>T, NC_000016.9(NM_024598.3):c.98+6G>T (USB1))

Chromosome 16
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.58035491G>T
DNA change (hg38) -
Published as USB1(NM_001204911.1):c.98+6G>T
ISCN -
DB-ID ZNF319_000011
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF319 NM_020807.1 -?/. - c.-2352C>A r.(?) p.(=)
USB1 NM_024598.3 -?/. - c.98+6G>T r.(=) p.(=)


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