Colon Cancer: Gene >> CORO1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341356
Start	67438419:67438419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2286624
CDS Mutation	c.1427G>A
AA Mutation	p.Arg476His(p.R476H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341356
Start	67442004:67442004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769428845
CDS Mutation	c.286G>A
AA Mutation	p.Glu96Lys(p.E96K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341356
Start	67442059:67442059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567987315
CDS Mutation	c.231G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341356
Start	67441149:67441149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.732G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341356
Start	67440371:67440371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143585970
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341356
Start	67440341:67440341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140493861
CDS Mutation	c.855C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341356
Start	67441510:67441510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369102459
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341356
Start	67441492:67441492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CORO1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341356
Start	67441452:67441452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517A>G
AA Mutation	p.Ser173Gly(p.S173G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000341356
Start	67441406:67441407(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.545_562dupTCAGCTGGAACCACAATG
AA Mutation	p.Val182_Asn187dup(p.V182_N187dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript