Variant #0000334950 (NC_000023.10:g.101909051A>T, ARMCX5(NM_022838.3):c.*50305A>T)

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.101909051A>T
DNA change (hg38) g.102654123A>T
Published as GPRASP1(NM_001099411.1):c.210A>T (p.(=))
ISCN -
DB-ID ARMCX5-GPRASP2_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARMCX5-GPRASP2 NM_001199818.1 ?/. - c.-480+48470A>T r.(=) p.(=)
GPRASP1 NM_014710.4 ?/. - c.210A>T r.(?) p.(Ala70=)
ARMCX5 NM_022838.3 ?/. - c.*50305A>T r.(=) p.(=)
GPRASP2 NM_138437.5 ?/. - c.-58909A>T r.(?) p.(=)