Colon Cancer: Gene >> TSSK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399635
Start	19131632:19131632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.233T>C
AA Mutation	p.Ile78Thr(p.I78T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399635
Start	19132298:19132298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899A>G
AA Mutation	p.Asp300Gly(p.D300G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399635
Start	19131886:19131886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371638010
CDS Mutation	c.487C>T
AA Mutation	p.Arg163Trp(p.R163W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399635
Start	19132033:19132033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634G>A
AA Mutation	p.Gly212Ser(p.G212S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399635
Start	19132162:19132162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763C>T
AA Mutation	p.Pro255Ser(p.P255S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399635
Start	19132446:19132446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200682587
CDS Mutation	c.1047C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TSSK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399635
Start	19132192:19132192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793G>A
AA Mutation	p.Glu265Lys(p.E265K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399635
Start	19131529:19131529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755276601
CDS Mutation	c.130G>A
AA Mutation	p.Asp44Asn(p.D44N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript