Variant #0000866991 (NC_000023.10:g.11272778G>A, NM_013427.2:c.638C>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.11272778G>A
DNA change (hg38) -
Published as ARHGAP6(NM_013427.2):c.638C>T (p.S213L)
ISCN -
DB-ID ARHGAP6_000053
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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP6 NM_013427.2 ?/. - c.638C>T r.(?) p.(Ser213Leu)
AMELX NM_182680.1 ?/. - c.-38823G>A r.(?) p.(=)


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