Colon Cancer: Gene >> MAN1C1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374332
Start	25686497:25686497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147313933
CDS Mutation	c.598C>T
AA Mutation	p.Arg200Cys(p.R200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374332
Start	25763952:25763952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1126G>A
AA Mutation	p.Gly376Arg(p.G376R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374332
Start	25749258:25749258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760511398
CDS Mutation	c.757G>A
AA Mutation	p.Gly253Arg(p.G253R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374332
Start	25618221:25618221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Cys(p.R142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374332
Start	25686471:25686471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755018052
CDS Mutation	c.572G>A
AA Mutation	p.Arg191His(p.R191H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374332
Start	25618255:25618255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458G>A
AA Mutation	p.Arg153His(p.R153H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374332
Start	25763941:25763941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115G>T
AA Mutation	p.Ser372Ile(p.S372I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374332
Start	25746781:25746781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751G>A
AA Mutation	p.Val251Met(p.V251M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374332
Start	25746708:25746708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374332
Start	25746702:25746702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142965225
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374332
Start	25763906:25763906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749676923
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000374332
Start	25780999:25780999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1537C>T
AA Mutation	p.Gln513Ter(p.Q513*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAN1C1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374332
Start	25781027:25781027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766513186
CDS Mutation	c.1565G>A
AA Mutation	p.Arg522Gln(p.R522Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374332
Start	25686516:25686516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617G>A
AA Mutation	p.Gly206Asp(p.G206D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374332
Start	25686491:25686491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592G>A
AA Mutation	p.Glu198Lys(p.E198K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374332
Start	25778233:25778233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756727309
CDS Mutation	c.1386C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374332
Start	25758631:25758631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.969C>A
Mutation Classification	Silent
Feature Type	Transcript