Colon Cancer: Gene >> SOCS6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397942
Start	70325936:70325936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268G>A
AA Mutation	p.Arg423His(p.R423H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397942
Start	70324966:70324966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298G>A
AA Mutation	p.Asp100Asn(p.D100N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397942
Start	70325972:70325972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1304A>G
AA Mutation	p.His435Arg(p.H435R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397942
Start	70326250:70326250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1582G>A
AA Mutation	p.Asp528Asn(p.D528N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397942
Start	70325690:70325690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769812956
CDS Mutation	c.1022G>A
AA Mutation	p.Arg341His(p.R341H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397942
Start	70325449:70325449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754658030
CDS Mutation	c.781G>A
AA Mutation	p.Ala261Thr(p.A261T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397942
Start	70325568:70325568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184346343
CDS Mutation	c.900G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397942
Start	70324859:70324860(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.197dupA
AA Mutation	p.Asn66LysfsTer49(p.N66Kfs*49)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SOCS6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397942
Start	70325424:70325424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751363744
CDS Mutation	c.756G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397942
Start	70325508:70325508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41535447
CDS Mutation	c.840C>T
Mutation Classification	Silent
Feature Type	Transcript