Colon Cancer: Gene >> TRIM41

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315073
Start	181224682:181224682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683C>A
AA Mutation	p.Pro228His(p.P228H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315073
Start	181234615:181234615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532938397
CDS Mutation	c.1733G>A
AA Mutation	p.Arg578His(p.R578H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315073
Start	181232692:181232692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943T>C
AA Mutation	p.Ser315Pro(p.S315P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315073
Start	181234483:181234483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755074419
CDS Mutation	c.1601G>A
AA Mutation	p.Arg534His(p.R534H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315073
Start	181234536:181234536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1654G>A
AA Mutation	p.Val552Met(p.V552M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315073
Start	181232719:181232719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.970C>G
AA Mutation	p.Leu324Val(p.L324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315073
Start	181232667:181232667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918G>T
AA Mutation	p.Met306Ile(p.M306I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315073
Start	181234666:181234666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1784C>A
AA Mutation	p.Ala595Glu(p.A595E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315073
Start	181224227:181224227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.228G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315073
Start	181224185:181224185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315073
Start	181234574:181234574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1692C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315073
Start	181234565:181234565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1683C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315073
Start	181234369:181234381(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs758265545
CDS Mutation	c.1490_1502delGCTGGGCGGTGGG
AA Mutation	p.Gly497ValfsTer70(p.G497Vfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM41

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315073
Start	181234233:181234233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772110248
CDS Mutation	c.1351C>T
AA Mutation	p.Arg451Trp(p.R451W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315073
Start	181224714:181224714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715G>A
AA Mutation	p.Glu239Lys(p.E239K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315073
Start	181234307:181234307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1425A>G
Mutation Classification	Silent
Feature Type	Transcript