Variant #0000866942 (NC_000023.10:g.101970240C>T, ARMCX5(NM_022838.3):c.*111494C>T)

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.101970240C>T
DNA change (hg38) -
Published as GPRASP2(NM_001184874.2):c.443C>T (p.T148I)
ISCN -
DB-ID ARMCX5_000035
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARMCX5-GPRASP2 NM_001199818.1 -?/. - c.443C>T r.(?) p.(Thr148Ile)
GPRASP1 NM_014710.4 -?/. - c.*57211C>T r.(=) p.(=)
ARMCX5 NM_022838.3 -?/. - c.*111494C>T r.(=) p.(=)
GPRASP2 NM_138437.5 -?/. - c.443C>T r.(?) p.(Thr148Ile)