Variant #0000993267 (NC_000003.11:g.128853002C>A, NM_020701.3:c.578G>T (ISY1))

Chromosome 3
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.128853002C>A
DNA change (hg38) -
Published as ISY1(NM_020701.3):c.578G>T (p.(Arg193Ile))
ISCN -
DB-ID ISY1_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB43 NM_001204883.1 -?/. - c.-12058G>T r.(?) p.(=)
ISY1-RAB43 NM_001204890.1 -?/. - c.578G>T r.(?) p.(Arg193Ile)
ISY1 NM_020701.3 -?/. - c.578G>T r.(?) p.(Arg193Ile)


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