Variant #0001043998 (NC_000023.10:g.101857535A>G, NM_022838.3:c.466A>G (ARMCX5))

Chromosome X
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.101857535A>G
DNA change (hg38) -
Published as ARMCX5(NM_001168478.2):c.466A>G (p.(Thr156Ala))
ISCN -
DB-ID ARMCX5_000006 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) 0.00338 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     
ARMCX5-GPRASP2 NM_001199818.1 -/. - c.-652+1098A>G r.(=) p.(=)
GPRASP1 NM_014710.4 -/. - c.-49560A>G r.(?) p.(=)
ARMCX5 NM_022838.3 -/. - c.466A>G r.(?) p.(Thr156Ala)
GPRASP2 NM_138437.5 -/. - c.-110425A>G r.(?) p.(=)


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