Variant #0000542897 (NC_000011.9:g.125773062T>C, NC_000011.9(NM_031307.3):c.-47+3A>G (PUS3))

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.125773062T>C
DNA change (hg38) g.125903167T>C
Published as PUS3(NM_001271985.1):c.-247+3A>G (p.(=))
ISCN -
DB-ID HYLS1_000006 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-01 16:22:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HYLS1 NM_001134793.1 -?/. - c.*2899T>C r.(=) p.(=)
DDX25 NM_013264.4 -?/. - c.-1351T>C r.(?) p.(=)
PUS3 NM_031307.3 -?/. - c.-47+3A>G r.spl? p.?
HYLS1 NM_145014.2 -?/. - c.*2899T>C r.(=) p.(=)


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