Variant #0000866943 (NC_000023.10:g.101971255C>T, ARMCX5(NM_022838.3):c.*112509C>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.101971255C>T
DNA change (hg38) -
Published as ARMCX5-GPRASP2(NM_001199818.1):c.1458C>T (p.S486=), GPRASP2(NM_001184874.2):c.1458C>T (p.S486=)
ISCN -
DB-ID ARMCX5_000036
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) Variant not found in online data sets
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.1458C>T r.(?) p.(Ser486=)
GPRASP1 NM_014710.4 -?/. - c.*58226C>T r.(=) p.(=)
ARMCX5 NM_022838.3 -?/. - c.*112509C>T r.(=) p.(=)
BHLHB9 NM_030639.2 -?/. - c.-4927C>T r.(?) p.(=)
GPRASP2 NM_138437.5 -?/. - c.1458C>T r.(?) p.(Ser486=)