Variant #0000915636 (NC_000023.10:g.153171704_153171715del, ARHGAP4(NM_001666.4):c.*1473_*1484del)

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.153171704_153171715del
DNA change (hg38) -
Published as AVPR2(NM_000054.6):c.744_755delCAGGGGACGCCG (p.R249_R252del), AVPR2(NM_001146151.2):c.744_755delCAGGGGACGCCG (p.R249_R252del), AVPR2(NM_001146151....)
ISCN -
DB-ID AVPR2_000011 See all 3 reported entries
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.744_755del r.(?) p.(Arg249_Arg252del)
ARHGAP4 NM_001666.4 -?/. - c.*1473_*1484del r.(=) p.(=)