Variant #0000718793 (NC_000002.11:g.44059195G>C, NM_022436.2:c.293C>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.44059195G>C
DNA change (hg38) -
Published as ABCG5(NM_022436.2):c.293C>G (p.A98G), ABCG5(NM_022436.3):c.293C>G (p.A98G)
ISCN -
DB-ID ABCG5_000043 See all 5 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) 0.00236 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYNC2LI1 NM_016008.3 -/. - c.*22289G>C r.(=) p.(=)
ABCG5 NM_022436.2 -/. - c.293C>G r.(?) p.(Ala98Gly)


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