Colon Cancer: Gene >> GALNT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356317
Start	51365453:51365453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791T>G
AA Mutation	p.Val264Gly(p.V264G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356317
Start	51360777:51360777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1111A>G
AA Mutation	p.Thr371Ala(p.T371A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356317
Start	51377222:51377222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637A>G
AA Mutation	p.Ile213Val(p.I213V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356317
Start	51360738:51360738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1150G>A
AA Mutation	p.Val384Met(p.V384M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356317
Start	51355927:51355927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752182003
CDS Mutation	c.1634G>A
AA Mutation	p.Arg545His(p.R545H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356317
Start	51364276:51364276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.894C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356317
Start	51360739:51360739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138065864
CDS Mutation	c.1149C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356317
Start	51360829:51360829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147006309
CDS Mutation	c.1059G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356317
Start	51364246:51364246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370958932
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356317
Start	51359294:51359294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356317
Start	51357370:51357370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1581C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356317
Start	51357394:51357394(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs770106085
CDS Mutation	c.1557delG
AA Mutation	p.Lys520SerfsTer79(p.K520Sfs*79)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GALNT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356317
Start	51360746:51360746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142G>A
AA Mutation	p.Gly381Glu(p.G381E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356317
Start	51379727:51379727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751132786
CDS Mutation	c.55G>A
AA Mutation	p.Ala19Thr(p.A19T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript