Colon Cancer: Gene >> DLX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222598
Start	97021060:97021060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546A>C
AA Mutation	p.Lys182Asn(p.K182N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222598
Start	97020914:97020914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142492086
CDS Mutation	c.692G>A
AA Mutation	p.Arg231His(p.R231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222598
Start	97022225:97022225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500G>A
AA Mutation	p.Arg167His(p.R167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222598
Start	97024556:97024556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68C>A
AA Mutation	p.Thr23Lys(p.T23K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222598
Start	97024490:97024490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134C>A
AA Mutation	p.Ser45Tyr(p.S45Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222598
Start	97022246:97022246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.479A>G
AA Mutation	p.Gln160Arg(p.Q160R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222598
Start	97024344:97024344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>A
AA Mutation	p.Asp94Asn(p.D94N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222598
Start	97022312:97022312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413G>A
AA Mutation	p.Arg138His(p.R138H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222598
Start	97020940:97020940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222598
Start	97024372:97024372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61753628
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222598
Start	97024555:97024555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.69G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222598
Start	97020820:97020820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222598
Start	97024466:97024466(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.158delG
AA Mutation	p.Gly53GlufsTer28(p.G53Efs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DLX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222598
Start	97022225:97022225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500G>A
AA Mutation	p.Arg167His(p.R167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222598
Start	97020915:97020915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691C>T
AA Mutation	p.Arg231Cys(p.R231C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222598
Start	97024486:97024486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222598
Start	97024534:97024534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222598
Start	97020922:97020922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684C>G
Mutation Classification	Silent
Feature Type	Transcript