Colon Cancer: Gene >> CLDN18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000183605
Start	138010370:138010370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145C>T
AA Mutation	p.Leu49Phe(p.L49F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000183605
Start	138024642:138024642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421A>G
AA Mutation	p.Asn141Asp(p.N141D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000183605
Start	138024609:138024609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388C>A
AA Mutation	p.Leu130Ile(p.L130I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000183605
Start	138029866:138029866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573G>A
AA Mutation	p.Met191Ile(p.M191I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343735
Start	137999005:137999005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137A>T
AA Mutation	p.Tyr46Phe(p.Y46F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000183605
Start	138024622:138024622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401C>T
AA Mutation	p.Ala134Val(p.A134V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000183605
Start	138010302:138010302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77G>A
AA Mutation	p.Gly26Glu(p.G26E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000343735
Start	137998986:137998986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369029508
CDS Mutation	c.118G>A
AA Mutation	p.Val40Ile(p.V40I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000183605
Start	138024641:138024641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000183605
Start	138023675:138023675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761116930
CDS Mutation	c.238C>T
AA Mutation	p.Arg80Ter(p.R80*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CLDN18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000183605
Start	138010306:138010306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.81G>A
AA Mutation	p.Met27Ile(p.M27I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343735
Start	137998962:137998962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94A>C
AA Mutation	p.Thr32Pro(p.T32P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343735
Start	137998892:137998892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24C>T
Mutation Classification	Silent
Feature Type	Transcript