Colon Cancer: Gene >> ST8SIA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396037
Start	22287287:22287287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243A>C
AA Mutation	p.Gln81His(p.Q81H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396037
Start	22287216:22287216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314T>C
AA Mutation	p.Met105Thr(p.M105T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396037
Start	22255368:22255368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403T>G
AA Mutation	p.Leu135Val(p.L135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396037
Start	22249013:22249013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755554035
CDS Mutation	c.577C>T
AA Mutation	p.Arg193Trp(p.R193W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396037
Start	22201814:22201814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809C>A
AA Mutation	p.Ala270Asp(p.A270D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396037
Start	22201797:22201797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.826G>A
AA Mutation	p.Gly276Arg(p.G276R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396037
Start	22255356:22255356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415G>A
AA Mutation	p.Ala139Thr(p.A139T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396037
Start	22201612:22201612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375498016
CDS Mutation	c.1011C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396037
Start	22334173:22334173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396037
Start	22334071:22334071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396037
Start	22334032:22334032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142528967
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396037
Start	22334052:22334052(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.181delG
AA Mutation	p.Val61CysfsTer34(p.V61Cfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ST8SIA1

No Mutation Annotation!