Colon Cancer: Gene >> GALNT11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000430044
Start	152094429:152094429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746809374
CDS Mutation	c.202G>A
AA Mutation	p.Glu68Lys(p.E68K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000430044
Start	152103222:152103222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771748654
CDS Mutation	c.530G>A
AA Mutation	p.Arg177His(p.R177H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000430044
Start	152094297:152094297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70C>T
AA Mutation	p.Leu24Phe(p.L24F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000430044
Start	152117274:152117274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1351G>A
AA Mutation	p.Val451Ile(p.V451I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000430044
Start	152108137:152108137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812G>A
AA Mutation	p.Cys271Tyr(p.C271Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000430044
Start	152120885:152120885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184763995
CDS Mutation	c.1612G>C
AA Mutation	p.Asp538His(p.D538H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000430044
Start	152105323:152105323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201883939
CDS Mutation	c.665G>A
AA Mutation	p.Arg222His(p.R222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430044
Start	152108180:152108180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.855C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430044
Start	152094458:152094458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199933998
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430044
Start	152120860:152120860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755243433
CDS Mutation	c.1587G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430044
Start	152113338:152113338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1173C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000430044
Start	152094383:152094383(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.162delA
AA Mutation	p.Lys54AsnfsTer26(p.K54Nfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000430044
Start	152100812:152100812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>T
AA Mutation	p.Glu104Ter(p.E104*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GALNT11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000430044
Start	152094361:152094361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.134C>T
AA Mutation	p.Ser45Phe(p.S45F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript