Colon Cancer: Gene >> CD40LG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370629
Start	136648255:136648255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>A
AA Mutation	p.Glu3Lys(p.E3K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370629
Start	136659378:136659378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749G>T
AA Mutation	p.Gly250Val(p.G250V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370629
Start	136654430:136654430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346G>T
AA Mutation	p.Gly116Cys(p.G116C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370629
Start	136659153:136659153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524T>C
AA Mutation	p.Val175Ala(p.V175A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370629
Start	136648296:136648296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.48A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370629
Start	136659043:136659043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.414A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370629
Start	136654399:136654399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778398894
CDS Mutation	c.315G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370629
Start	136656399:136656399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370629
Start	136648337:136648337(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.93delT
AA Mutation	p.Ile33SerfsTer4(p.I33Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CD40LG

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370629
Start	136659283:136659283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368157256
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript