Variant #0008781500 (NC_000014.8:g.51368584T>C, NM_002863.4:c.*3526A>G (PYGL))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.51368584T>C
DB-ID -
dbSNP ID rs140167439
gnomAD frequency 113/228024
gnomAD homozygote count 0/113898
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PYGL NM_001163940.1 ./. c.*3526A>G r.(=) p.(=)
ABHD12B NM_001206673.1 ./. c.818delTinsC r.(?) p.(Met273Thr)
PYGL NM_002863.4 ./. c.*3526A>G r.(=) p.(=)
ABHD12B NM_181814.1 ./. c.587delTinsC r.(?) p.(Met196Thr)