Colon Cancer: Gene >> TSPYL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277330:97277330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515C>T
AA Mutation	p.Ala172Val(p.A172V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277517:97277517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328G>A
AA Mutation	p.Ala110Thr(p.A110T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277704:97277704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141C>A
AA Mutation	p.Asp47Glu(p.D47E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277234:97277234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611C>T
AA Mutation	p.Thr204Met(p.T204M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277507:97277507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338C>T
AA Mutation	p.Ser113Leu(p.S113L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277060:97277060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.785T>C
AA Mutation	p.Leu262Pro(p.L262P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322128
Start	97277836:97277836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322128
Start	97277434:97277434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774166479
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322128
Start	97277479:97277479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322128
Start	97277311:97277311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780774946
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322128
Start	97277444:97277444(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.401delA
AA Mutation	p.Asn134MetfsTer30(p.N134Mfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322128
Start	97277436:97277436(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.409delC
AA Mutation	p.Arg137AlafsTer27(p.R137Afs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TSPYL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97276718:97276718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1127A>T
AA Mutation	p.Asn376Ile(p.N376I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277460:97277460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115912728
CDS Mutation	c.385G>A
AA Mutation	p.Val129Met(p.V129M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97276950:97276950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895G>A
AA Mutation	p.Asp299Asn(p.D299N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000322128
Start	97277145:97277145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Ter(p.R234*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript