Variant #0000923771 (NC_000002.11:g.61128137T>C, NM_144709.2:c.*41393A>G (PUS10))

Chromosome 2
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.61128137T>C
DNA change (hg38) -
Published as REL(NM_002908.4):c.313T>C (p.L105=)
ISCN -
DB-ID PUS10_000002
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) 0.00014 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 2023-04-16 21:50:28 +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     
REL NM_002908.2 -?/. - c.313T>C r.(?) p.(Leu105=)
PUS10 NM_144709.2 -?/. - c.*41393A>G r.(=) p.(=)


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