Colon Cancer: Gene >> LGR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71553179:71553179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565985845
CDS Mutation	c.535G>A
AA Mutation	p.Val179Ile(p.V179I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71583844:71583844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765873009
CDS Mutation	c.1834G>A
AA Mutation	p.Val612Met(p.V612M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71583680:71583680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1670G>A
AA Mutation	p.Gly557Asp(p.G557D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71504631:71504631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230A>G
AA Mutation	p.Asn77Ser(p.N77S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71553183:71553183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539A>C
AA Mutation	p.Gln180Pro(p.Q180P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71578871:71578871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348T>G
AA Mutation	p.Leu450Val(p.L450V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71583655:71583655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645A>C
AA Mutation	p.Lys549Gln(p.K549Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71553087:71553087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443A>G
AA Mutation	p.Asn148Ser(p.N148S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000266674
Start	71440291:71440291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211C>A
AA Mutation	p.Leu71Ile(p.L71I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266674
Start	71584275:71584275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2265C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266674
Start	71583846:71583846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1836G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266674
Start	71584581:71584581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2571C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266674
Start	71440182:71440182(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.105delC
AA Mutation	p.Thr36HisfsTer36(p.T36Hfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266674
Start	71583932:71583933(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1928dupT
AA Mutation	p.Leu643PhefsTer31(p.L643Ffs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LGR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71584198:71584198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2188A>T
AA Mutation	p.Ile730Phe(p.I730F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71535124:71535124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366G>T
AA Mutation	p.Gln122His(p.Q122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266674
Start	71553117:71553117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473T>G
AA Mutation	p.Phe158Cys(p.F158C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266674
Start	71571574:71571574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1131G>A
Mutation Classification	Silent
Feature Type	Transcript