Colon Cancer: Gene >> PGGT1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419445
Start	115253236:115253236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755476746
CDS Mutation	c.160G>A
AA Mutation	p.Ala54Thr(p.A54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419445
Start	115236394:115236394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608G>C
AA Mutation	p.Ser203Thr(p.S203T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000419445
Start	115212560:115212560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976A>C
AA Mutation	p.Ile326Leu(p.I326L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000419445
Start	115216941:115216941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876G>T
AA Mutation	p.Glu292Asp(p.E292D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419445
Start	115262786:115262786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000419445
Start	115221945:115221946(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.721dupT
AA Mutation	p.Ser241PhefsTer25(p.S241Ffs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PGGT1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419445
Start	115262795:115262795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57T>A
AA Mutation	p.Asp19Glu(p.D19E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000419445
Start	115221955:115221955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712G>T
AA Mutation	p.Glu238Ter(p.E238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript