Variant #0000951790 (NC_000023.10:g.69497391C>G, NC_000023.10(NM_004312.2):c.609+12C>G (ARR3))

Chromosome X
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.69497391C>G
DNA change (hg38) -
Published as ARR3(NM_004312.3):c.609+12C>G
ISCN -
DB-ID ARR3_000044
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) 0.00192 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB41 NM_001032726.2 -?/. - c.-4677C>G r.(?) p.(=)
ARR3 NM_004312.2 -?/. - c.609+12C>G r.(=) p.(=)


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