Colon Cancer: Gene >> CLDN8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399899
Start	30215292:30215292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634G>A
AA Mutation	p.Gly212Arg(p.G212R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399899
Start	30215661:30215661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265G>A
AA Mutation	p.Val89Met(p.V89M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399899
Start	30215319:30215319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367879638
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Cys(p.R203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399899
Start	30215845:30215845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81G>A
AA Mutation	p.Met27Ile(p.M27I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399899
Start	30215491:30215491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399899
Start	30215536:30215536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399899
Start	30215860:30215860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399899
Start	30215852:30215853(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.73_74insGTCCT
AA Mutation	p.Thr25SerfsTer30(p.T25Sfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	start_lost
Transcription ID	ENST00000399899
Start	30215925:30215925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1A>T
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CLDN8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399899
Start	30215640:30215640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286A>G
AA Mutation	p.Met96Val(p.M96V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399899
Start	30215770:30215770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156G>C
AA Mutation	p.Met52Ile(p.M52I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000399899
Start	30215907:30215907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19G>T
AA Mutation	p.Glu7Ter(p.E7*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript