Colon Cancer: Gene >> SPATS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321898
Start	49526040:49526040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423C>T
AA Mutation	p.Arg475Cys(p.R475C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321898
Start	49500127:49500127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377665993
CDS Mutation	c.761G>A
AA Mutation	p.Arg254Gln(p.R254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321898
Start	49494790:49494790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314G>A
AA Mutation	p.Gly105Asp(p.G105D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000321898
Start	49490730:49490730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263A>C
AA Mutation	p.Lys88Thr(p.K88T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321898
Start	49494789:49494789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749730463
CDS Mutation	c.313G>A
AA Mutation	p.Gly105Ser(p.G105S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321898
Start	49526038:49526038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1421G>T
AA Mutation	p.Gly474Val(p.G474V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321898
Start	49494845:49494845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321898
Start	49519149:49519149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000321898
Start	49500178:49500179(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.812_813insTAATTATAT
AA Mutation	p.Lys271delinsAsnAsnTyrIle(p.K271delinsNNYI)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	start_lost
Transcription ID	ENST00000321898
Start	49461014:49461014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SPATS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321898
Start	49524891:49524891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321C>T
AA Mutation	p.Arg441Trp(p.R441W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript