Variant #0000969287 (NC_000017.10:g.79892801del, NC_000017.10(NM_006907.2):c.540+1del (PYCR1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.79892801del
DNA change (hg38) -
Published as PYCR1(NM_006907.4):c.540+1delG
ISCN -
DB-ID MYADML2_000010
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYADML2 NM_001145113.2 +/. - c.*5893del r.(?) p.(=)
PYCR1 NM_006907.2 +/. - c.540+1del r.spl? p.?


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