Variant #0000333157 (NC_000023.10:g.11206891G>A, NM_013427.2:c.1034C>T (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.11206891G>A
DNA change (hg38) g.11188771G>A
Published as ARHGAP6(NM_006125.2):c.1034C>T (p.(Thr345Met))
ISCN -
DB-ID ARHGAP6_000023
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) 1.0E-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 2018-01-15 20:58:59 +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.1034C>T r.(?) p.(Thr345Met)
AMELX NM_182680.1 ?/. - c.-104710G>A r.(?) p.(=)


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