Colon Cancer: Gene >> TRIM25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316881
Start	56904376:56904376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.806G>T
AA Mutation	p.Arg269Met(p.R269M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316881
Start	56891731:56891731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1862G>A
AA Mutation	p.Gly621Asp(p.G621D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316881
Start	56892016:56892016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577T>C
AA Mutation	p.Val526Ala(p.V526A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316881
Start	56891966:56891966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1627G>A
AA Mutation	p.Gly543Ser(p.G543S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316881
Start	56913427:56913427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763430514
CDS Mutation	c.562C>T
AA Mutation	p.Pro188Ser(p.P188S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316881
Start	56891927:56891927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1666A>G
AA Mutation	p.Thr556Ala(p.T556A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316881
Start	56892123:56892123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142382736
CDS Mutation	c.1470G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316881
Start	56899164:56899164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759955328
CDS Mutation	c.1104T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316881
Start	56901426:56901426(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1080delC
AA Mutation	p.Ser361ValfsTer20(p.S361Vfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316881
Start	56908515:56908515(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746988951
CDS Mutation	c.646delG
AA Mutation	p.Ala216ArgfsTer8(p.A216Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316881
Start	56913526:56913527(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.462_463insTTTGCGC
AA Mutation	p.Arg155PhefsTer32(p.R155Ffs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316881
Start	56892144:56892144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1449G>T
AA Mutation	p.Glu483Asp(p.E483D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316881
Start	56904266:56904266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747508258
CDS Mutation	c.916G>A
AA Mutation	p.Glu306Lys(p.E306K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript