Genomic variant #0000574160

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.150912824C>A
DNA change (hg38) g.151744352C>A
Published as CNGA2(NM_005140.1):c.1849C>A (p.(Arg617Ser))
ISCN -
DB-ID CNGA2_000035
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNGA2 NM_005140.1 ?/. - c.1849C>A r.(?) p.(Arg617Ser)