Variant #0000763597 (NC_000011.9:g.64519395C>T, NC_000011.9(NM_005609.2):c.1768+1G>A (PYGM))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.64519395C>T
DNA change (hg38) g.64751923C>T
Published as -
ISCN -
DB-ID PYGM_000010 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Irene Vieitez
Database submission license No license selected
Created by Irene Vieitez
Date created 2021-04-12 14:00:11 +02:00 (CEST)
Date last edited 2021-04-12 14:01:18 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PYGM NM_005609.2 +/. - c.1768+1G>A r.spl p.?


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