Variant #0000693250 (NC_000023.10:g.101857876T>G, ARMCX5(NM_022838.3):c.807T>G)

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.101857876T>G
DNA change (hg38) -
Published as ARMCX5(NM_001168479.1):c.807T>G (p.P269=)
ISCN -
DB-ID ARMCX5_000026
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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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+1439T>G r.(=) p.(=)
GPRASP1 NM_014710.4 -?/. - c.-49219T>G r.(?) p.(=)
ARMCX5 NM_022838.3 -?/. - c.807T>G r.(?) p.(Pro269=)
GPRASP2 NM_138437.5 -?/. - c.-110084T>G r.(?) p.(=)