Variant #0000351379 (NC_000017.10:g.79892524C>T, NC_000017.10(NM_006907.2):c.633+5G>A (PYCR1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.79892524C>T
DNA change (hg38) g.81934648C>T
Published as -
ISCN -
DB-ID PYCR1_000022
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-14 16:04:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYADML2 NM_001145113.2 +?/. - c.*6170G>A r.(=) p.(=)
PYCR1 NM_006907.2 +?/. - c.633+5G>A r.spl? p.?


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