Colon Cancer: Gene >> SARS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221431
Start	38921646:38921646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541776059
CDS Mutation	c.415C>T
AA Mutation	p.Arg139Trp(p.R139W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221431
Start	38930681:38930681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.56G>A
AA Mutation	p.Arg19Gln(p.R19Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221431
Start	38917931:38917931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040A>G
AA Mutation	p.His347Arg(p.H347R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221431
Start	38930554:38930554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183G>T
AA Mutation	p.Glu61Asp(p.E61D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221431
Start	38916083:38916083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1301A>G
AA Mutation	p.His434Arg(p.H434R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221431
Start	38917752:38917752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1132A>G
AA Mutation	p.Ile378Val(p.I378V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221431
Start	38915708:38915708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377315322
CDS Mutation	c.1455C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221431
Start	38918130:38918131(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.925_926insGGTGC
AA Mutation	p.Met309ArgfsTer50(p.M309Rfs*50)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SARS2

No Mutation Annotation!