Variant #0000542898 (NC_000011.9:g.125775498A>G, NM_031307.3:c.-2480T>C (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.125775498A>G
DNA change (hg38) g.125905603A>G
Published as DDX25(NM_013264.4):c.175+6A>G (p.(=))
ISCN -
DB-ID HYLS1_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) 3.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HYLS1 NM_001134793.1 -?/. - c.*5335A>G r.(=) p.(=)
DDX25 NM_013264.4 -?/. - c.175+6A>G r.(=) p.(=)
PUS3 NM_031307.3 -?/. - c.-2480T>C r.(?) p.(=)
HYLS1 NM_145014.2 -?/. - c.*5335A>G r.(=) p.(=)


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