Colon Cancer: Gene >> TPX2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000300403
Start	31783919:31783919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1411G>T
AA Mutation	p.Val471Leu(p.V471L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31801004:31801004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2168G>A
AA Mutation	p.Gly723Asp(p.G723D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31797502:31797502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1932G>T
AA Mutation	p.Lys644Asn(p.K644N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31766565:31766565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239C>T
AA Mutation	p.Thr80Ile(p.T80I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31777570:31777570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814C>T
AA Mutation	p.Pro272Ser(p.P272S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31757480:31757480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4T>C
AA Mutation	p.Ser2Pro(p.S2P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31793947:31793947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1609C>A
AA Mutation	p.Pro537Thr(p.P537T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31770403:31770403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417A>C
AA Mutation	p.Lys139Asn(p.K139N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31777619:31777619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746496077
CDS Mutation	c.863G>A
AA Mutation	p.Arg288Gln(p.R288Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300403
Start	31793856:31793856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759746158
CDS Mutation	c.1518C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000300403
Start	31766588:31766588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.262G>T
AA Mutation	p.Glu88Ter(p.E88*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000300403
Start	31794007:31794007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1669G>T
AA Mutation	p.Glu557Ter(p.E557*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TPX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31760124:31760124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174A>T
AA Mutation	p.Lys58Asn(p.K58N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript