Genomic variant #0000557668

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.2522122T>A
DNA change (hg38) -
Published as NTN3(NM_006181.2):c.420T>A (p.(His140Gln))
ISCN -
DB-ID TBC1D24_000088
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




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
TBC1D24 NM_001199107.1 ?/. - c.-3165T>A VUS r.(?) p.(=)
NTN3 NM_006181.2 ?/. - c.420T>A VUS r.(?) p.(His140Gln)
TBC1D24 NM_020705.2 ?/. - c.-3165T>A VUS r.(?) p.(=)
C16orf59 NM_025108.2 ?/. - c.*7453T>A VUS r.(=) p.(=)