Variant #0000257061 (NC_000002.11:g.44047136T>C, NM_022436.2:c.1567A>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.44047136T>C
DNA change (hg38) g.43819997T>C
Published as ABCG5(NM_022436.3):c.1567A>G (p.I523V), DYNC2LI1(NM_001348913.2):c.*16-7389T>C
ISCN -
DB-ID ABCG5_000010 See all 2 reported entries
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) 0.00171 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.*10230T>C r.(=) p.(=)
ABCG5 NM_022436.2 -/. - c.1567A>G r.(?) p.(Ile523Val)


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