Colon Cancer: Gene >> MOS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113646:56113646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337C>T
AA Mutation	p.Arg113Cys(p.R113C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113370:56113370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613G>A
AA Mutation	p.Ala205Thr(p.A205T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113492:56113492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.491A>G
AA Mutation	p.Glu164Gly(p.E164G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113858:56113858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125G>A
AA Mutation	p.Arg42Gln(p.R42Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113048:56113048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935G>A
AA Mutation	p.Arg312His(p.R312H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113604:56113604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379A>C
AA Mutation	p.Thr127Pro(p.T127P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113096:56113096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.887G>A
AA Mutation	p.Arg296His(p.R296H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113684:56113684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299G>A
AA Mutation	p.Arg100Gln(p.R100Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113738:56113738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.245T>C
AA Mutation	p.Val82Ala(p.V82A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56112989:56112989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761563451
CDS Mutation	c.994C>T
AA Mutation	p.Arg332Trp(p.R332W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113771:56113771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212T>G
AA Mutation	p.Phe71Cys(p.F71C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113421:56113421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562G>A
AA Mutation	p.Gly188Ser(p.G188S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113888:56113888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95C>T
AA Mutation	p.Ala32Val(p.A32V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311923
Start	56113323:56113323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311923
Start	56112993:56112993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311923
Start	56113602:56113602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MOS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113658:56113658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>A
AA Mutation	p.Val109Ile(p.V109I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113462:56113462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521G>C
AA Mutation	p.Ser174Thr(p.S174T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113082:56113082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901G>A
AA Mutation	p.Ala301Thr(p.A301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113739:56113739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244G>A
AA Mutation	p.Val82Ile(p.V82I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript