TP53TG3C

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

Effect	PathogenicP	Likely pathogenicLP	VUS	Likely benignLB	BenignB
synonymous
missense
nonsense
start loss
frameshift
splice donor/acceptor (+/-2bp)
Total	0	0	0	0	0

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Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 4 of 8 transcripts

Transcript ID	Source	Protein ID	Coding Exons	MANE Status
NM_001205259.3	RefSeq	NP_001192188.1	2	MANE Select
ENST00000561509.3	Ensembl	ENSP00000455132.1	2	MANE Select
ENST00000360260.6	Ensembl	ENSP00000353397.2	2	Standard
ENST00000567137.1	Ensembl	ENSP00000454442.1	2	Standard

dbNSFP Gene Annotations

Source: dbNSFP

Function: FUNCTION: May play a significant role in p53/TP53-mediating signaling pathway. {ECO:0000269|PubMed:10534768}.;

Essentials

Essential (CRISPR): E
Essential (gene trap): N
Indispensability pred.: N
Indispensability score: 0.114