Variant #0000574458 (NC_000023.10:g.153196209C>T, ARHGAP4(NM_001666.4):c.-4553G>A)

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.153196209C>T
DNA change (hg38) g.153930756C>T
Published as NAA10(NM_001256119.1):c.426+7G>A (p.(=)), NAA10(NM_003491.3):c.471+7G>A
ISCN -
DB-ID NAA10_000012 See all 2 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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP4 NM_001666.4 -?/. - c.-4553G>A r.(?) p.(=)
RENBP NM_002910.5 -?/. - c.*4530G>A r.(=) p.(=)
NAA10 NM_003491.3 -?/. - c.471+7G>A r.(=) p.(=)