Colon Cancer: Gene >> LIG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108208858:108208858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2411C>T
AA Mutation	p.Ser804Phe(p.S804F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108209227:108209227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2042G>T
AA Mutation	p.Arg681Ile(p.R681I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108208941:108208941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2328A>T
AA Mutation	p.Glu776Asp(p.E776D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108208963:108208963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761592929
CDS Mutation	c.2306C>T
AA Mutation	p.Thr769Ile(p.T769I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108208733:108208733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778998772
CDS Mutation	c.2536C>T
AA Mutation	p.Arg846Trp(p.R846W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108208821:108208821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2448C>G
AA Mutation	p.His816Gln(p.H816Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108210319:108210319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950A>G
AA Mutation	p.Asn317Ser(p.N317S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108209722:108209722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547A>G
AA Mutation	p.Tyr516Cys(p.Y516C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356922
Start	108209178:108209178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184527984
CDS Mutation	c.2091G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356922
Start	108209439:108209439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768563098
CDS Mutation	c.1830C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356922
Start	108209478:108209478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144253952
CDS Mutation	c.1791C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356922
Start	108210763:108210763(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.506delA
AA Mutation	p.Lys169ArgfsTer7(p.K169Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000356922
Start	108209015:108209015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2254G>T
AA Mutation	p.Glu752Ter(p.E752*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356922
Start	108209883:108209884(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1385dupT
AA Mutation	p.Leu462PhefsTer12(p.L462Ffs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LIG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108211093:108211093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176A>G
AA Mutation	p.Asp59Gly(p.D59G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108210156:108210156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1113G>C
AA Mutation	p.Met371Ile(p.M371I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108211070:108211070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Ala67Thr(p.A67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108209179:108209179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2090C>T
AA Mutation	p.Thr697Met(p.T697M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356922
Start	108209268:108209268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2001G>C
AA Mutation	p.Met667Ile(p.M667I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356922
Start	108209784:108209784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1485G>A
Mutation Classification	Silent
Feature Type	Transcript