Colon Cancer: Gene >> IL6ST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55964173:55964173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631C>T
AA Mutation	p.His211Tyr(p.H211Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55956120:55956120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172T>A
AA Mutation	p.Leu391His(p.L391H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55947551:55947551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879T>G
AA Mutation	p.Leu627Val(p.L627V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55964190:55964190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614G>A
AA Mutation	p.Gly205Glu(p.G205E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000336909
Start	55956235:55956235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057A>G
AA Mutation	p.Thr353Ala(p.T353A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55941305:55941305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2534T>G
AA Mutation	p.Phe845Cys(p.F845C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55941524:55941524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768129650
CDS Mutation	c.2315C>T
AA Mutation	p.Pro772Leu(p.P772L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55969706:55969706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214T>G
AA Mutation	p.Phe72Val(p.F72V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55941578:55941578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2261C>T
AA Mutation	p.Ser754Leu(p.S754L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55956088:55956088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1204G>A
AA Mutation	p.Val402Ile(p.V402I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336909
Start	55941427:55941427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200386892
CDS Mutation	c.2412C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336909
Start	55952041:55952041(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776023104
CDS Mutation	c.1587delA
AA Mutation	p.Val530Ter(p.V530*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336909
Start	55941649:55941649(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2190delG
AA Mutation	p.Ser731LeufsTer57(p.S731Lfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336909
Start	55941731:55941732(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2107_2108insAGAT
AA Mutation	p.Pro703GlnfsTer19(p.P703Qfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IL6ST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55941099:55941099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2740G>A
AA Mutation	p.Gly914Ser(p.G914S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55941178:55941178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2661A>C
AA Mutation	p.Arg887Ser(p.R887S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336909
Start	55957280:55957280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985G>T
AA Mutation	p.Ala329Ser(p.A329S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript