Variant #0001016053 (NC_000023.10:g.69500654C>G, NM_004312.2:c.1052C>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.69500654C>G
DNA change (hg38) -
Published as ARR3(NM_004312.2):c.1052C>G (p.P351R), ARR3(NM_004312.3):c.1052C>G (p.P351R)
ISCN -
DB-ID ARR3_000040 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) 0.0016 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 2024-10-29 21:08:56 +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.-1414C>G r.(?) p.(=)
ARR3 NM_004312.2 -?/. - c.1052C>G r.(?) p.(Pro351Arg)


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