Colon Cancer: Gene >> B4GALNT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341156
Start	57628853:57628853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774565348
CDS Mutation	c.862C>T
AA Mutation	p.Arg288Cys(p.R288C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341156
Start	57627840:57627840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1162G>A
AA Mutation	p.Glu388Lys(p.E388K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341156
Start	57627663:57627663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1339C>T
AA Mutation	p.Arg447Cys(p.R447C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341156
Start	57626865:57626865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1481G>T
AA Mutation	p.Arg494Met(p.R494M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341156
Start	57631055:57631055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415G>T
AA Mutation	p.Ala139Ser(p.A139S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341156
Start	57626899:57626899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1447C>T
AA Mutation	p.His483Tyr(p.H483Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341156
Start	57628831:57628831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.884T>G
AA Mutation	p.Leu295Arg(p.L295R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341156
Start	57628130:57628130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151177784
CDS Mutation	c.1135C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341156
Start	57628197:57628197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341156
Start	57631211:57631211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341156
Start	57631320:57631320(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs745744124
CDS Mutation	c.263delG
AA Mutation	p.Gly88AlafsTer24(p.G88Afs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341156
Start	57631319:57631320(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs778572229
CDS Mutation	c.263dupG
AA Mutation	p.Leu89ProfsTer13(p.L89Pfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> B4GALNT1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341156
Start	57628254:57628254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759167970
CDS Mutation	c.1011C>T
Mutation Classification	Silent
Feature Type	Transcript