Variant #0000572984 (NC_000023.10:g.109560826C>G, NM_020769.2:c.-101705C>G (RGAG1))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.109560826C>G
DNA change (hg38) g.110317598C>G
Published as AMMECR1(NM_001171689.1):c.104+1G>C
ISCN -
DB-ID RGAG1_000032
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-21 08:43:35 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMMECR1 NM_001025580.1 +/. - c.473+1G>C r.spl? p.?
RGAG1 NM_020769.2 +/. - c.-101705C>G r.(?) p.(=)


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