Colon Cancer: Gene >> GALNT13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154396110:154396110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150203694
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Cys(p.R426C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154301469:154301469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1036C>T
AA Mutation	p.Arg346Trp(p.R346W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154396108:154396108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274G>T
AA Mutation	p.Arg425Ile(p.R425I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154140479:154140479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285A>T
AA Mutation	p.Arg95Ser(p.R95S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154242758:154242758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539T>G
AA Mutation	p.Ile180Ser(p.I180S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	153944628:153944628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.131C>T
AA Mutation	p.Pro44Leu(p.P44L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154242058:154242058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340C>A
AA Mutation	p.Leu114Ile(p.L114I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154245919:154245919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751205543
CDS Mutation	c.794G>A
AA Mutation	p.Arg265His(p.R265H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	153944579:153944579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82T>C
AA Mutation	p.Phe28Leu(p.F28L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154242757:154242757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149581963
CDS Mutation	c.538A>G
AA Mutation	p.Ile180Val(p.I180V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154242703:154242703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484C>A
AA Mutation	p.Leu162Ile(p.L162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154242892:154242892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673A>C
AA Mutation	p.Ile225Leu(p.I225L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154140430:154140430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236A>C
AA Mutation	p.Lys79Thr(p.K79T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154409007:154409007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1320G>T
AA Mutation	p.Gln440His(p.Q440H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392825
Start	154301489:154301489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1056T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392825
Start	153944620:153944620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392825
Start	154450449:154450449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1569C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392825
Start	154396085:154396085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1251C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392825
Start	154301426:154301426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000392825
Start	154245942:154245942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817G>T
AA Mutation	p.Glu273Ter(p.E273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000392825
Start	154438661:154438661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1465G>T
AA Mutation	p.Gly489Ter(p.G489*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GALNT13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154409027:154409027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1340G>A
AA Mutation	p.Arg447His(p.R447H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	153944511:153944511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14T>C
AA Mutation	p.Val5Ala(p.V5A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154245979:154245979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.854T>C
AA Mutation	p.Val285Ala(p.V285A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392825
Start	154301565:154301565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1132G>T
AA Mutation	p.Asp378Tyr(p.D378Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000392825
Start	154245942:154245942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817G>T
AA Mutation	p.Glu273Ter(p.E273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript