Variant #0000245945 (NC_000002.11:g.44040455A>C, NC_000002.11(NM_022436.2):c.1763-7T>G (ABCG5))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44040455A>C
DNA change (hg38) g.43813316A>C
Published as ABCG5(NM_022436.3):c.1763-7T>G, DYNC2LI1(NM_001348913.2):c.*15+2792A>C
ISCN -
DB-ID ABCG5_000053
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) 0.00065 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYNC2LI1 NM_016008.3 -/. - c.*3549A>C r.(=) p.(=)
ABCG5 NM_022436.2 -/. - c.1763-7T>G r.(=) p.(=)


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