Colon Cancer: Gene >> CUL4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375440
Start	113242980:113242980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048G>A
AA Mutation	p.Ala350Thr(p.A350T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375440
Start	113253118:113253118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1675C>G
AA Mutation	p.Leu559Val(p.L559V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375440
Start	113235117:113235117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201623121
CDS Mutation	c.820G>A
AA Mutation	p.Val274Ile(p.V274I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375440
Start	113253116:113253116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1673A>G
AA Mutation	p.Tyr558Cys(p.Y558C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375440
Start	113255120:113255120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2026G>A
AA Mutation	p.Glu676Lys(p.E676K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375440
Start	113228030:113228030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375440
Start	113242982:113242982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771623025
CDS Mutation	c.1050G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375440
Start	113245008:113245009(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1395_1396delAA
AA Mutation	p.Ser466CysfsTer6(p.S466Cfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CUL4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375440
Start	113244981:113244981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366G>A
AA Mutation	p.Asp456Asn(p.D456N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375440
Start	113242985:113242985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146783617
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript