Variant #0004389332 (NC_000006.11:g.43415058C>A, NM_033450.2:c.3533delCinsA (ABCC10))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43415058C>A
DB-ID -
dbSNP ID rs746070362
gnomAD frequency 1/245660
gnomAD homozygote count 0/122826
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     
ABCC10 NM_001198934.1 ./. c.3617delCinsA r.(?) p.(Thr1206Lys)
DLK2 NM_023932.2 ./. c.*3219G>T r.(=) p.(=)
ABCC10 NM_033450.2 ./. c.3533delCinsA r.(?) p.(Thr1178Lys)
DLK2 NM_206539.1 ./. c.*3219G>T r.(=) p.(=)