Variant #0000528922 (NC_000006.11:g.43402544C>T, NM_033450.2:c.1437C>T (ABCC10))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43402544C>T
DNA change (hg38) g.43434806C>T
Published as ABCC10(NM_033450.2):c.1437C>T (p.F479=)
ISCN -
DB-ID ABCC10_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 13:31:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLK2 NM_023932.2 -?/. - c.*15733G>A r.(=) p.(=)
ABCC10 NM_033450.2 -?/. - c.1437C>T r.(?) p.(Phe479=)


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