Variant #0008781584 (NC_000014.8:g.51370773C>T, NM_002863.4:c.*1337G>A (PYGL))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.51370773C>T
DB-ID -
dbSNP ID rs757911675
gnomAD frequency 2/238960
gnomAD homozygote count 0/119475
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.*1337G>A r.(=) p.(=)
ABHD12B NM_001206673.1 ./. c.943-19delCinsT r.(=) p.(=)
PYGL NM_002863.4 ./. c.*1337G>A r.(=) p.(=)
ABHD12B NM_181814.1 ./. c.712-19delCinsT r.(=) p.(=)