Colon Cancer: Gene >> SEMA6C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151142549:151142549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373129237
CDS Mutation	c.73G>A
AA Mutation	p.Ala25Thr(p.A25T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151135296:151135296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150793383
CDS Mutation	c.1447C>T
AA Mutation	p.Arg483Trp(p.R483W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151139682:151139682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253G>T
AA Mutation	p.Asp85Tyr(p.D85Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151132576:151132576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2701G>A
AA Mutation	p.Asp901Asn(p.D901N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000341697
Start	151135592:151135592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766594931
CDS Mutation	c.1432C>T
AA Mutation	p.Arg478Trp(p.R478W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151137005:151137005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826C>A
AA Mutation	p.His276Asn(p.H276N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151142584:151142584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38T>G
AA Mutation	p.Leu13Arg(p.L13R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151139477:151139477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302T>C
AA Mutation	p.Leu101Pro(p.L101P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151136969:151136969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.862T>A
AA Mutation	p.Ser288Thr(p.S288T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151139435:151139435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344G>A
AA Mutation	p.Gly115Glu(p.G115E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151132702:151132702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762830558
CDS Mutation	c.2575G>C
AA Mutation	p.Ala859Pro(p.A859P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341697
Start	151136564:151136564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755089884
CDS Mutation	c.990C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341697
Start	151135686:151135686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1338T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341697
Start	151135243:151135243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765494648
CDS Mutation	c.1500T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341697
Start	151136459:151136459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341697
Start	151142525:151142525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341697
Start	151138723:151138723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341697
Start	151132695:151132695(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2582delC
AA Mutation	p.Pro861LeufsTer37(p.P861Lfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000341697
Start	151142555:151142555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67C>T
AA Mutation	p.Gln23Ter(p.Q23*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SEMA6C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151138710:151138710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376C>T
AA Mutation	p.Arg126Cys(p.R126C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151139670:151139670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143410634
CDS Mutation	c.265G>A
AA Mutation	p.Glu89Lys(p.E89K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341697
Start	151134804:151134804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652C>A
AA Mutation	p.Ser551Tyr(p.S551Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript