Colon Cancer: Gene >> AKR1B10

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359579
Start	134538275:134538275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823C>A
AA Mutation	p.Gln275Lys(p.Q275K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359579
Start	134538965:134538965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.856A>C
AA Mutation	p.Met286Leu(p.M286L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359579
Start	134530656:134530656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80A>C
AA Mutation	p.Lys27Thr(p.K27T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359579
Start	134541049:134541049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563438026
CDS Mutation	c.911C>T
AA Mutation	p.Ser304Phe(p.S304F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359579
Start	134537080:134537080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373551927
CDS Mutation	c.582G>T
AA Mutation	p.Glu194Asp(p.E194D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359579
Start	134533040:134533040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388A>T
AA Mutation	p.Asn130Tyr(p.N130Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359579
Start	134541057:134541057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359579
Start	134537122:134537122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568011657
CDS Mutation	c.624G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359579
Start	134539009:134539009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376662494
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359579
Start	134537643:134537644(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.730dupA
AA Mutation	p.Thr244AsnfsTer29(p.T244Nfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359579
Start	134537091:134537092(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.593_594insCT
AA Mutation	p.Gln198HisfsTer53(p.Q198Hfs*53)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000359579
Start	134537092:134537093(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.594_595insAGA
AA Mutation	p.Gln198_Tyr199insArg(p.Q198_Y199insR)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> AKR1B10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359579
Start	134531986:134531986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313C>A
AA Mutation	p.Leu105Met(p.L105M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359579
Start	134537122:134537122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568011657
CDS Mutation	c.624G>A
Mutation Classification	Silent
Feature Type	Transcript