Variant #0000728351 (NC_000023.10:g.11207028G>A, ARHGAP6(NM_013427.2):c.897C>T)

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11207028G>A
DNA change (hg38) -
Published as ARHGAP6(NM_013427.2):c.897C>T (p.D299=)
ISCN -
DB-ID ARHGAP6_000049
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP6 NM_013427.2 -?/. - c.897C>T r.(?) p.(Asp299=)
AMELX NM_182680.1 -?/. - c.-104573G>A r.(?) p.(=)