Variant #0001006296 (NC_000023.10:g.101972156A>G, NM_022838.3:c.*113410A>G (ARMCX5))

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.101972156A>G
DNA change (hg38) -
Published as GPRASP2(NM_138437.5):c.2359A>G (p.(Ile787Val))
ISCN -
DB-ID ARMCX5_000040
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.2359A>G r.(?) p.(Ile787Val)
GPRASP1 NM_014710.4 ?/. - c.*59127A>G r.(=) p.(=)
ARMCX5 NM_022838.3 ?/. - c.*113410A>G r.(=) p.(=)
BHLHB9 NM_030639.2 ?/. - c.-4026A>G r.(?) p.(=)
GPRASP2 NM_138437.5 ?/. - c.2359A>G r.(?) p.(Ile787Val)


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