Variant #0004389644 (NC_000006.11:g.43417249G>C, NM_033450.2:c.4209delGinsC (ABCC10))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43417249G>C
DB-ID -
dbSNP ID rs757938316
gnomAD frequency 1/246090
gnomAD homozygote count 0/123042
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.4293delGinsC r.(?) p.(Lys1431Asn)
DLK2 NM_023932.2 ./. c.*1028C>G r.(=) p.(=)
ABCC10 NM_033450.2 ./. c.4209delGinsC r.(?) p.(Lys1403Asn)
DLK2 NM_206539.1 ./. c.*1028C>G r.(=) p.(=)