Colon Cancer: Gene >> STC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173323259:173323259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466A>T
AA Mutation	p.Ile156Leu(p.I156L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173318011:173318011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745C>A
AA Mutation	p.Pro249Thr(p.P249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173318041:173318041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715C>A
AA Mutation	p.His239Asn(p.H239N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173317948:173317948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373237346
CDS Mutation	c.808G>A
AA Mutation	p.Ala270Thr(p.A270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173317854:173317854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775448844
CDS Mutation	c.902G>A
AA Mutation	p.Arg301Gln(p.R301Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173317956:173317956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800A>G
AA Mutation	p.His267Arg(p.H267R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173323370:173323370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Gly119Ser(p.G119S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173325897:173325897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>A
AA Mutation	p.Leu89Met(p.L89M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173323284:173323284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765087494
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173318039:173318039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771024676
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173328116:173328116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173325949:173325949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147198518
CDS Mutation	c.213C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173323287:173323287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775095401
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173318180:173318180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000265087
Start	173323408:173323422(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.303_317delATTCATCAAAGACGC
AA Mutation	p.Phe102_Ala106del(p.F102_A106del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STC2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173325874:173325874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173328173:173328173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript