Colon Cancer: Gene >> GALNT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392701
Start	165748852:165748852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1831G>C
AA Mutation	p.Glu611Gln(p.E611Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392701
Start	165749822:165749822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1699G>T
AA Mutation	p.Gly567Cys(p.G567C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392701
Start	165748830:165748830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1853G>A
AA Mutation	p.Cys618Tyr(p.C618Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392701
Start	165749863:165749863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201855584
CDS Mutation	c.1658G>A
AA Mutation	p.Arg553Gln(p.R553Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392701
Start	165759456:165759456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.953A>C
AA Mutation	p.Lys318Thr(p.K318T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392701
Start	165754970:165754970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773423949
CDS Mutation	c.1486G>T
AA Mutation	p.Val496Leu(p.V496L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392701
Start	165764973:165764973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138645426
CDS Mutation	c.599C>T
AA Mutation	p.Thr200Met(p.T200M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392701
Start	165770195:165770195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377319905
CDS Mutation	c.506G>A
AA Mutation	p.Arg169Gln(p.R169Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392701
Start	165761941:165761941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752243721
CDS Mutation	c.802G>A
AA Mutation	p.Ala268Thr(p.A268T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392701
Start	165755020:165755020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767939917
CDS Mutation	c.1436G>A
AA Mutation	p.Arg479His(p.R479H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392701
Start	165749799:165749799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1722T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392701
Start	165770443:165770443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392701
Start	165748805:165748805(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1878delA
AA Mutation	p.Lys626AsnfsTer16(p.K626Nfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392701
Start	165770575:165770578(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.123_126delAAGT
AA Mutation	p.Ser42PhefsTer14(p.S42Ffs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000392701
Start	165757110:165757110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1329G>A
AA Mutation	p.Trp443Ter(p.W443*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_lost
Transcription ID	ENST00000392701
Start	165748781:165748781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1902A>C
AA Mutation	p.Ter634TyrextTer18(p.*634Yext*18)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GALNT3

No Mutation Annotation!