Variant #0000615708 (NC_000016.9:g.1497456G>C, CLCN7(NM_001287.5):c.2187C>G)

Chromosome 16
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.1497456G>C
DNA change (hg38) g.1447455G>C
Published as CLCN7(NM_001287.5):c.2187C>G (p.D729E)
ISCN -
DB-ID CCDC154_000015
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_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC154 NM_001143980.1 -?/. - c.-3133C>G r.(?) p.(=)
CLCN7 NM_001287.5 -?/. - c.2187C>G r.(?) p.(Asp729Glu)