Colon Cancer: Gene >> TPCN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335509
Start	113273589:113273589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863C>A
AA Mutation	p.Pro288His(p.P288H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335509
Start	113273235:113273235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.787T>C
AA Mutation	p.Phe263Leu(p.F263L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335509
Start	113268778:113268778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565G>A
AA Mutation	p.Val189Met(p.V189M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335509
Start	113273259:113273259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>A
AA Mutation	p.Val271Ile(p.V271I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335509
Start	113273618:113273618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368144508
CDS Mutation	c.892G>A
AA Mutation	p.Val298Ile(p.V298I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335509
Start	113272672:113272672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.763T>C
AA Mutation	p.Ser255Pro(p.S255P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335509
Start	113296000:113296000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2375G>A
AA Mutation	p.Arg792Gln(p.R792Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000335509
Start	113266237:113266237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295G>A
AA Mutation	p.Ala99Thr(p.A99T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000335509
Start	113273601:113273601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875G>A
AA Mutation	p.Arg292Gln(p.R292Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335509
Start	113287011:113287011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756074282
CDS Mutation	c.1551C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335509
Start	113269808:113269808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335509
Start	113288193:113288193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538285886
CDS Mutation	c.1665C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335509
Start	113287032:113287032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs12322533
CDS Mutation	c.1572G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335509
Start	113277020:113277020(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1044delG
AA Mutation	p.Leu349SerfsTer26(p.L349Sfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000335509
Start	113296002:113296002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2377C>T
AA Mutation	p.Gln793Ter(p.Q793*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TPCN1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335509
Start	113293313:113293313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759494751
CDS Mutation	c.2298C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335509
Start	113260480:113260480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.225A>C
Mutation Classification	Silent
Feature Type	Transcript