Colon Cancer: Gene >> LMTK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48502466:48502466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761T>C
AA Mutation	p.Leu254Pro(p.L254P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48502442:48502442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.785A>G
AA Mutation	p.Tyr262Cys(p.Y262C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48497767:48497767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3302C>T
AA Mutation	p.Ala1101Val(p.A1101V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48499403:48499403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1666G>A
AA Mutation	p.Asp556Asn(p.D556N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48501005:48501005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142C>T
AA Mutation	p.Ala381Val(p.A381V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48502480:48502480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747G>C
AA Mutation	p.Glu249Asp(p.E249D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48499082:48499082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1987C>T
AA Mutation	p.Arg663Cys(p.R663C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48497821:48497821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3248C>T
AA Mutation	p.Thr1083Met(p.T1083M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000600059
Start	48499689:48499689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000600059
Start	48502477:48502477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000600059
Start	48499737:48499737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1332G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000600059
Start	48491489:48491489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4143G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000600059
Start	48498024:48498024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3045G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000600059
Start	48498369:48498369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2700C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000600059
Start	48509499:48509499(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.376delC
AA Mutation	p.Leu126TrpfsTer8(p.L126Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000600059
Start	48498440:48498440(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2629delG
AA Mutation	p.Glu877ArgfsTer27(p.E877Rfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000600059
Start	48498957:48498957(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2112delC
AA Mutation	p.Glu705ArgfsTer153(p.E705Rfs*153)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000600059
Start	48491501:48491501(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs777732799
CDS Mutation	c.4131delC
AA Mutation	p.Glu1378ArgfsTer106(p.E1378Rfs*106)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000600059
Start	48501405:48501405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LMTK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48510473:48510473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196G>A
AA Mutation	p.Asp66Asn(p.D66N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48499204:48499204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1865C>T
AA Mutation	p.Ala622Val(p.A622V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000600059
Start	48508897:48508897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511G>A
AA Mutation	p.Gly171Arg(p.G171R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000600059
Start	48498240:48498240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2829G>A
Mutation Classification	Silent
Feature Type	Transcript