Colon Cancer: Gene >> TEKT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10682083:10682083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773C>T
AA Mutation	p.Ser258Leu(p.S258L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10694612:10694612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138237208
CDS Mutation	c.262C>T
AA Mutation	p.Arg88Cys(p.R88C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10694630:10694630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774554761
CDS Mutation	c.244C>T
AA Mutation	p.Arg82Cys(p.R82C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10635803:10635803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549750185
CDS Mutation	c.1202G>A
AA Mutation	p.Arg401His(p.R401H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10635845:10635845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759487224
CDS Mutation	c.1160C>T
AA Mutation	p.Pro387Leu(p.P387L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10694611:10694611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768273976
CDS Mutation	c.263G>A
AA Mutation	p.Arg88His(p.R88H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10682041:10682041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201580847
CDS Mutation	c.815C>T
AA Mutation	p.Thr272Met(p.T272M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10694472:10694472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402G>T
AA Mutation	p.Gln134His(p.Q134H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10694653:10694653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747708531
CDS Mutation	c.221C>T
AA Mutation	p.Pro74Leu(p.P74L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283025
Start	10694820:10694820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283025
Start	10694547:10694547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283025
Start	10694625:10694625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370028779
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283025
Start	10694679:10694679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775658432
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000283025
Start	10681992:10681992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748580746
CDS Mutation	c.863+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TEKT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10694611:10694611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768273976
CDS Mutation	c.263G>A
AA Mutation	p.Arg88His(p.R88H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283025
Start	10694585:10694585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289T>C
AA Mutation	p.Ser97Pro(p.S97P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283025
Start	10682070:10682070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148685770
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript