Colon Cancer: Gene >> SS18L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331758
Start	62164214:62164214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.791C>T
AA Mutation	p.Ala264Val(p.A264V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331758
Start	62174568:62174568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1088G>A
AA Mutation	p.Gly363Asp(p.G363D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331758
Start	62165473:62165473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875A>G
AA Mutation	p.Asp292Gly(p.D292G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331758
Start	62174622:62174622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142A>G
AA Mutation	p.Gln381Arg(p.Q381R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331758
Start	62158745:62158745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746253864
CDS Mutation	c.143C>T
AA Mutation	p.Thr48Met(p.T48M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331758
Start	62143826:62143826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331758
Start	62165510:62165510(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.916+1delG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SS18L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331758
Start	62163511:62163511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753325512
CDS Mutation	c.610G>A
AA Mutation	p.Gly204Ser(p.G204S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331758
Start	62164218:62164218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.795G>A
Mutation Classification	Silent
Feature Type	Transcript