Colon Cancer: Gene >> SND1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127929276:127929276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143989011
CDS Mutation	c.1616G>A
AA Mutation	p.Arg539His(p.R539H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127807503:127807503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771628442
CDS Mutation	c.1172G>A
AA Mutation	p.Arg391His(p.R391H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128086960:128086960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139075193
CDS Mutation	c.2327G>A
AA Mutation	p.Arg776His(p.R776H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127694863:127694863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264G>T
AA Mutation	p.Lys88Asn(p.K88N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127703230:127703230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.747A>T
AA Mutation	p.Lys249Asn(p.K249N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128084805:128084805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552426263
CDS Mutation	c.2192G>A
AA Mutation	p.Arg731His(p.R731H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127844334:127844334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200994299
CDS Mutation	c.1253C>T
AA Mutation	p.Thr418Met(p.T418M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127929237:127929237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577G>A
AA Mutation	p.Arg526His(p.R526H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128089669:128089669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2599A>G
AA Mutation	p.Lys867Glu(p.K867E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128074659:128074659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1937C>T
AA Mutation	p.Ala646Val(p.A646V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	127703180:127703180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697C>T
AA Mutation	p.Arg233Trp(p.R233W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128085715:128085715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369890577
CDS Mutation	c.2239C>T
AA Mutation	p.Arg747Cys(p.R747C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	128074624:128074624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1902C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	127702490:127702490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	127844335:127844335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751946216
CDS Mutation	c.1254G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354725
Start	127929195:127929195(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1539delA
AA Mutation	p.Ala514GlnfsTer156(p.A514Qfs*156)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000354725
Start	127704854:127704854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>T
AA Mutation	p.Glu286Ter(p.E286*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000354725
Start	128092003:128092003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2678G>A
AA Mutation	p.Trp893Ter(p.W893*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000354725
Start	128081423:128081423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2032C>T
AA Mutation	p.Arg678Ter(p.R678*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	splice_acceptor_variant;intron_variant
Transcription ID	ENST00000354725
Start	128091963:128091992(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2668-30_2668-1delTGAAGAGCTATTGTCTGTTTTTTCTTACAG
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SND1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354725
Start	128089505:128089505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2435A>G
AA Mutation	p.Asp812Gly(p.D812G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354725
Start	127904762:127904762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1470C>T
Mutation Classification	Silent
Feature Type	Transcript