Variant #0001006295 (NC_000023.10:g.101910774T>C, NM_022838.3:c.*52028T>C (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.101910774T>C
DNA change (hg38) -
Published as GPRASP1(NM_001184727.1):c.1933T>C (p.(Cys645Arg))
ISCN -
DB-ID ARMCX5_000039
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.-480+50193T>C r.(=) p.(=)
GPRASP1 NM_014710.4 ?/. - c.1933T>C r.(?) p.(Cys645Arg)
ARMCX5 NM_022838.3 ?/. - c.*52028T>C r.(=) p.(=)
GPRASP2 NM_138437.5 ?/. - c.-57186T>C r.(?) p.(=)


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