Variant #0000261347 (NC_000023.10:g.153171451G>T, ARHGAP4(NM_001666.4):c.*1732C>A)

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.153171451G>T
DNA change (hg38) g.153905997G>T
Published as AVPR2(NM_000054.6):c.491G>T (p.W164L)
ISCN -
DB-ID AVPR2_000010
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.491G>T r.(?) p.(Trp164Leu)
ARHGAP4 NM_001666.4 +?/. - c.*1732C>A r.(=) p.(=)