Colon Cancer: Gene >> CCNE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262643
Start	29822109:29822109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.819A>C
AA Mutation	p.Gln273His(p.Q273H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262643
Start	29813001:29813001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144A>C
AA Mutation	p.Lys48Asn(p.K48N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262643
Start	29823764:29823764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147896943
CDS Mutation	c.1220C>T
AA Mutation	p.Pro407Leu(p.P407L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262643
Start	29822491:29822491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998C>T
AA Mutation	p.Pro333Leu(p.P333L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262643
Start	29822499:29822499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748914866
CDS Mutation	c.1006A>G
AA Mutation	p.Met336Val(p.M336V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262643
Start	29822091:29822091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262643
Start	29823732:29823732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754411380
CDS Mutation	c.1188G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262643
Start	29817275:29817275(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.319delG
AA Mutation	p.Val107TyrfsTer2(p.V107Yfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CCNE1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262643
Start	29820773:29820773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368794196
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript