Colon Cancer: Gene >> SMTNL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399154
Start	57543636:57543636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546652152
CDS Mutation	c.634C>T
AA Mutation	p.Pro212Ser(p.P212S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399154
Start	57550087:57550087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1349G>T
AA Mutation	p.Gly450Val(p.G450V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399154
Start	57543073:57543073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431C>T
AA Mutation	p.Ala144Val(p.A144V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399154
Start	57546627:57546627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1204T>G
AA Mutation	p.Phe402Val(p.F402V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399154
Start	57546596:57546596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1173A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399154
Start	57546539:57546539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399154
Start	57546593:57546593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570413222
CDS Mutation	c.1170C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399154
Start	57542699:57542699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776778790
CDS Mutation	c.57G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000399154
Start	57546518:57546520(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1097_1099delTCT
AA Mutation	p.Phe366del(p.F366del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SMTNL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399154
Start	57546325:57546325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377159051
CDS Mutation	c.1055G>A
AA Mutation	p.Arg352Gln(p.R352Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399154
Start	57546594:57546594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778534246
CDS Mutation	c.1171G>A
AA Mutation	p.Ala391Thr(p.A391T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399154
Start	57550020:57550020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1282G>A
AA Mutation	p.Ala428Thr(p.A428T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript