Variant #0001044041 (NC_000023.10:g.109561086G>C, NM_020769.2:c.-101445G>C (RGAG1))

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.109561086G>C
DNA change (hg38) -
Published as AMMECR1(NM_015365.3):c.214C>G (p.(Pro72Ala))
ISCN -
DB-ID RGAG1_000065
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
AMMECR1 NM_001025580.1 ?/. - c.214C>G r.(?) p.(Pro72Ala)
RGAG1 NM_020769.2 ?/. - c.-101445G>C r.(?) p.(=)


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