Variant #0000261345 (NC_000023.10:g.153171270C>T, ARHGAP4(NM_001666.4):c.*1913G>A)

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.153171270C>T
DNA change (hg38) g.153905816C>T
Published as AVPR2(NM_000054.6):c.310C>T (p.R104C)
ISCN -
DB-ID AVPR2_000057
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AVPR2 NM_000054.4 +/. - c.310C>T r.(?) p.(Arg104Cys)
ARHGAP4 NM_001666.4 +/. - c.*1913G>A r.(=) p.(=)