Colon Cancer: Gene >> CKMT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81252753:81252753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548849398
CDS Mutation	c.211G>A
AA Mutation	p.Ala71Thr(p.A71T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81251265:81251265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133C>T
AA Mutation	p.Pro45Ser(p.P45S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81255089:81255089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544C>T
AA Mutation	p.Arg182Trp(p.R182W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81257822:81257822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751778272
CDS Mutation	c.845G>A
AA Mutation	p.Arg282Gln(p.R282Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81263578:81263578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102T>C
AA Mutation	p.Tyr368His(p.Y368H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254035
Start	81257748:81257748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254035
Start	81255115:81255115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183430744
CDS Mutation	c.570C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254035
Start	81259197:81259197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369979117
CDS Mutation	c.957G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254035
Start	81263565:81263565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760448224
CDS Mutation	c.1089G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000254035
Start	81259212:81259214(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.974_976delTAC
AA Mutation	p.Leu325del(p.L325del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CKMT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81257819:81257819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842A>C
AA Mutation	p.Lys281Thr(p.K281T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81266174:81266174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1176T>G
AA Mutation	p.Asn392Lys(p.N392K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81255090:81255090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368812686
CDS Mutation	c.545G>A
AA Mutation	p.Arg182Gln(p.R182Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81255011:81255011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551718764
CDS Mutation	c.466G>A
AA Mutation	p.Asp156Asn(p.D156N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000254035
Start	81255212:81255212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371191747
CDS Mutation	c.667G>A
AA Mutation	p.Asp223Asn(p.D223N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81259126:81259126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754984187
CDS Mutation	c.886C>T
AA Mutation	p.Arg296Trp(p.R296W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254035
Start	81257843:81257843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368743817
CDS Mutation	c.866G>A
AA Mutation	p.Arg289His(p.R289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254035
Start	81255178:81255178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140162798
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254035
Start	81263580:81263580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150638385
CDS Mutation	c.1104C>T
Mutation Classification	Silent
Feature Type	Transcript