Variant #0000573071 (NC_000023.10:g.11160419G>T, NM_013427.2:c.2191C>A (ARHGAP6))

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.11160419G>T
DNA change (hg38) g.11142299G>T
Published as ARHGAP6(NM_006125.2):c.*1559C>A (p.(=))
ISCN -
DB-ID ARHGAP6_000038
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) 0.00166 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 2019-07-18 18:22:55 +02:00 (CEST)
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.2191C>A r.(?) p.(Pro731Thr)
AMELX NM_182680.1 -?/. - c.-151182G>T r.(?) p.(=)


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