Colon Cancer: Gene >> TTYH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269346
Start	74253136:74253136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150383554
CDS Mutation	c.1315C>T
AA Mutation	p.Arg439Cys(p.R439C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269346
Start	74249985:74249985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199845337
CDS Mutation	c.980C>T
AA Mutation	p.Ala327Val(p.A327V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269346
Start	74260147:74260147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1543G>A
AA Mutation	p.Ala515Thr(p.A515T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269346
Start	74249059:74249059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853A>T
AA Mutation	p.Thr285Ser(p.T285S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269346
Start	74230909:74230909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.324C>A
AA Mutation	p.Phe108Leu(p.F108L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269346
Start	74249955:74249955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375427011
CDS Mutation	c.950G>A
AA Mutation	p.Arg317His(p.R317H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269346
Start	74250292:74250292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1051C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269346
Start	74237447:74237447(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.568delG
AA Mutation	p.Val190CysfsTer9(p.V190Cfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	start_lost
Transcription ID	ENST00000269346
Start	74213589:74213589(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 >> TTYH2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269346
Start	74237437:74237437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.558A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269346
Start	74253255:74253255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434C>A
Mutation Classification	Silent
Feature Type	Transcript