Variant #0001034954 (NC_000005.9:g.141035334A>G, NC_000005.9(NM_022481.5):c.3973-9T>C (ARAP3))

Chromosome 5
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.141035334A>G
DNA change (hg38) -
Published as ARAP3(NM_022481.6):c.3973-9T>C
ISCN -
DB-ID ARAP3_000020
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) 0.00206 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
ARAP3 NM_022481.5 -?/. - c.3973-9T>C r.(=) p.(=)
FCHSD1 NM_033449.2 -?/. - c.-4399T>C r.(?) p.(=)
RELL2 NM_173828.4 -?/. - c.*15098A>G r.(=) p.(=)


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