Colon Cancer: Gene >> IRX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394636
Start	54933679:54933679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258C>T
AA Mutation	p.His420Tyr(p.H420Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394636
Start	54932888:54932888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.640G>A
AA Mutation	p.Glu214Lys(p.E214K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394636
Start	54932573:54932573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325T>C
AA Mutation	p.Tyr109His(p.Y109H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394636
Start	54932556:54932556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308C>T
AA Mutation	p.Ala103Val(p.A103V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394636
Start	54932528:54932528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>T
AA Mutation	p.Ala94Ser(p.A94S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394636
Start	54932655:54932655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.407G>A
AA Mutation	p.Arg136His(p.R136H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394636
Start	54932753:54932753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Trp(p.R169W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394636
Start	54933659:54933659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238C>T
AA Mutation	p.Thr413Met(p.T413M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000394636
Start	54933637:54933637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216G>A
AA Mutation	p.Ala406Thr(p.A406T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394636
Start	54932518:54932518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394636
Start	54932749:54932749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537133516
CDS Mutation	c.501G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394636
Start	54933660:54933660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1239G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394636
Start	54932554:54932554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394636
Start	54933726:54933726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394636
Start	54933777:54933777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1356T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394636
Start	54932803:54932803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IRX5

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394636
Start	54932740:54932740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394636
Start	54932845:54932845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript