Colon Cancer: Gene >> TESPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54963923:54963923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474A>C
AA Mutation	p.Gln158His(p.Q158H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54963003:54963003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753442863
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Trp(p.R299W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54962475:54962475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1423C>T
AA Mutation	p.Arg475Trp(p.R475W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54962831:54962831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1067C>T
AA Mutation	p.Ser356Phe(p.S356F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54962717:54962717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181C>A
AA Mutation	p.Ser394Tyr(p.S394Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54962967:54962967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931A>G
AA Mutation	p.Ser311Gly(p.S311G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54962514:54962514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187244716
CDS Mutation	c.1384C>A
AA Mutation	p.Gln462Lys(p.Q462K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54963048:54963048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Trp(p.R284W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000316577
Start	54966389:54966389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346A>G
AA Mutation	p.Arg116Gly(p.R116G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54962897:54962897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1001C>A
AA Mutation	p.Ser334Tyr(p.S334Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54963008:54963008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371019313
CDS Mutation	c.890G>A
AA Mutation	p.Arg297Gln(p.R297Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54962862:54962862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1036C>T
AA Mutation	p.Pro346Ser(p.P346S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316577
Start	54962572:54962572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316577
Start	54966088:54966088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316577
Start	54973515:54973515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316577
Start	54962661:54962661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000316577
Start	54962664:54962664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234G>T
AA Mutation	p.Glu412Ter(p.E412*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TESPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54962636:54962636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148518799
CDS Mutation	c.1262C>T
AA Mutation	p.Thr421Met(p.T421M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54963846:54963846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751647202
CDS Mutation	c.551G>A
AA Mutation	p.Arg184Gln(p.R184Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316577
Start	54963090:54963090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808C>A
AA Mutation	p.Leu270Met(p.L270M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316577
Start	54962905:54962905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316577
Start	54962635:54962635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200398984
CDS Mutation	c.1263G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316577
Start	54962815:54962815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1083C>A
Mutation Classification	Silent
Feature Type	Transcript