Colon Cancer: Gene >> LDB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86679479:86679479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206T>G
AA Mutation	p.Ile69Ser(p.I69S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86718743:86718743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1874T>C
AA Mutation	p.Leu625Ser(p.L625S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86716669:86716669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1574G>A
AA Mutation	p.Gly525Asp(p.G525D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86716372:86716372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1277C>A
AA Mutation	p.Pro426His(p.P426H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86709952:86709952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758933764
CDS Mutation	c.1133C>T
AA Mutation	p.Pro378Leu(p.P378L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86718119:86718119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832C>T
AA Mutation	p.Ala611Val(p.A611V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86726181:86726181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2023C>A
AA Mutation	p.Pro675Thr(p.P675T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86718102:86718102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1815C>A
AA Mutation	p.Phe605Leu(p.F605L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86726175:86726175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45514002
CDS Mutation	c.2017G>A
AA Mutation	p.Asp673Asn(p.D673N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86692562:86692562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201689564
CDS Mutation	c.887G>A
AA Mutation	p.Arg296Gln(p.R296Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86718841:86718841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760563152
CDS Mutation	c.1972G>A
AA Mutation	p.Glu658Lys(p.E658K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361373
Start	86692040:86692040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361373
Start	86726207:86726207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377178682
CDS Mutation	c.2049C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361373
Start	86681783:86681783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778089838
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361373
Start	86679435:86679435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757856121
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361373
Start	86718825:86718825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139213290
CDS Mutation	c.1956C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361373
Start	86681639:86681639(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.529delG
AA Mutation	p.Ala177ProfsTer31(p.A177Pfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LDB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361373
Start	86681680:86681680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45487699
CDS Mutation	c.566C>T
AA Mutation	p.Ser189Leu(p.S189L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361373
Start	86732895:86732895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2103T>C
Mutation Classification	Silent
Feature Type	Transcript