Colon Cancer: Gene >> HMX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339992
Start	123150050:123150050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749C>T
AA Mutation	p.Ala250Val(p.A250V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339992
Start	123149927:123149927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626C>T
AA Mutation	p.Ser209Leu(p.S209L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339992
Start	123150029:123150029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752047204
CDS Mutation	c.728C>T
AA Mutation	p.Pro243Leu(p.P243L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339992
Start	123148490:123148490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112G>A
AA Mutation	p.Val38Ile(p.V38I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339992
Start	123149773:123149773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.472C>T
AA Mutation	p.Arg158Cys(p.R158C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339992
Start	123149977:123149977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>A
AA Mutation	p.Val226Met(p.V226M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000339992
Start	123149987:123149987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686C>T
AA Mutation	p.Pro229Leu(p.P229L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000339992
Start	123149590:123149590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289G>C
AA Mutation	p.Gly97Arg(p.G97R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339992
Start	123149706:123149706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.405G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339992
Start	123148414:123148414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339992
Start	123148438:123148438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339992
Start	123149637:123149637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339992
Start	123148622:123148622(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.249delC
AA Mutation	p.Ile84SerfsTer87(p.I84Sfs*87)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HMX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339992
Start	123148545:123148545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167C>A
AA Mutation	p.Pro56Gln(p.P56Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript