Variant #0000728352 (NC_000023.10:g.11316938C>G, NC_000023.10(NM_013427.2):c.589-44111G>C (ARHGAP6))

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.11316938C>G
DNA change (hg38) -
Published as AMELX(NM_182680.1):c.457C>G (p.P153A)
ISCN -
DB-ID ARHGAP6_000050
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP6 NM_013427.2 ?/. - c.589-44111G>C r.(=) p.(=)
AMELX NM_182680.1 ?/. - c.457C>G r.(?) p.(Pro153Ala)


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