Variant #0000615709 (NC_000016.9:g.1497708C>T, CLCN7(NM_001287.5):c.2021G>A)

Chromosome 16
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.1497708C>T
DNA change (hg38) g.1447707C>T
Published as -
ISCN -
DB-ID CCDC154_000016
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) 6.0E-5 View details
Owner VKGL-NL_Nijmegen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC154 NM_001143980.1 ?/. - c.-3385G>A r.(?) p.(=)
CLCN7 NM_001287.5 ?/. - c.2021G>A r.(?) p.(Arg674Gln)