All transcript variants in gene FAM98C

Information The variants shown are described using the NM_174905.3 transcript reference sequence.

1 entry on 1 page. Showing entry 1.
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Effect     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.875C>A likely benign r.(?) p.(Thr292Asn) g.38897674C>A - RASGRP4:NM_001146202.1:c.*3006G>T, NM_001146203.1:c.*3006G>T, … - FAM98C_000001 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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