Variant #0000610366 (NC_000006.11:g.43413630C>G, NM_033450.2:c.3240C>G (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.43413630C>G
DNA change (hg38) g.43445892C>G
Published as ABCC10(NM_033450.2):c.3240C>G (p.A1080=)
ISCN -
DB-ID ABCC10_000006
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) 0.0002 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-19 13:32:17 +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.*4647G>C r.(=) p.(=)
ABCC10 NM_033450.2 -?/. - c.3240C>G r.(?) p.(Ala1080=)


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