Colon Cancer: Gene >> TMIGD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328886
Start	30324975:30324975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481C>A
AA Mutation	p.Leu161Ile(p.L161I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328886
Start	30325016:30325016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440C>T
AA Mutation	p.Ala147Val(p.A147V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328886
Start	30329379:30329379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233C>A
AA Mutation	p.Ser78Tyr(p.S78Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328886
Start	30329414:30329414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328886
Start	30329456:30329456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000328886
Start	30324991:30324991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.465G>A
AA Mutation	p.Trp155Ter(p.W155*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000328886
Start	30324897:30324897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559A>T
AA Mutation	p.Lys187Ter(p.K187*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000328886
Start	30317191:30317191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TMIGD1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000328886
Start	30325094:30325094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362T>C
AA Mutation	p.Phe121Ser(p.F121S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328886
Start	30318864:30318864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690G>T
Mutation Classification	Silent
Feature Type	Transcript