Genomic variant #0000326414

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.38897674C>A
DNA change (hg38) -
Published as FAM98C(NM_174905.3):c.875C>A (p.(Thr292Asn))
ISCN -
DB-ID FAM98C_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
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     
RASGRP4 NM_170604.2 ?/. - c.*3006G>T VUS r.(=) p.(=)
FAM98C NM_174905.3 ?/. - c.875C>A VUS r.(?) p.(Thr292Asn)