Colon Cancer: Gene >> HTR2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258400
Start	231108674:231108674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1289A>C
AA Mutation	p.Lys430Thr(p.K430T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258400
Start	231113776:231113776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747647526
CDS Mutation	c.506G>A
AA Mutation	p.Arg169Gln(p.R169Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258400
Start	231109020:231109020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943A>C
AA Mutation	p.Thr315Pro(p.T315P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258400
Start	231123607:231123607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158A>T
AA Mutation	p.Lys53Ile(p.K53I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258400
Start	231108662:231108662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781269061
CDS Mutation	c.1301G>A
AA Mutation	p.Arg434Gln(p.R434Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258400
Start	231109008:231109008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377419999
CDS Mutation	c.955G>A
AA Mutation	p.Glu319Lys(p.E319K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258400
Start	231123593:231123593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172G>A
AA Mutation	p.Ala58Thr(p.A58T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000258400
Start	231108959:231108959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004T>G
AA Mutation	p.Leu335Arg(p.L335R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000258400
Start	231113742:231113742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.540G>A
AA Mutation	p.Trp180Ter(p.W180*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258400
Start	231108687:231108688(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs760960108
CDS Mutation	c.1275dupT
AA Mutation	p.Lys426Ter(p.K426*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HTR2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258400
Start	231108801:231108801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77982984
CDS Mutation	c.1162C>T
AA Mutation	p.Arg388Trp(p.R388W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258400
Start	231108729:231108729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234T>G
AA Mutation	p.Ser412Ala(p.S412A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript