Colon Cancer: Gene >> SCIN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297029
Start	12629115:12629115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212A>C
AA Mutation	p.Glu404Asp(p.E404D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297029
Start	12626773:12626773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171G>T
AA Mutation	p.Val391Leu(p.V391L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297029
Start	12652685:12652685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2118G>C
AA Mutation	p.Trp706Cys(p.W706C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000297029
Start	12636135:12636135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1410G>T
AA Mutation	p.Gln470His(p.Q470H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297029
Start	12644169:12644169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1613A>C
AA Mutation	p.Asn538Thr(p.N538T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297029
Start	12625776:12625776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907C>T
AA Mutation	p.Pro303Ser(p.P303S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297029
Start	12649475:12649475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1890G>T
AA Mutation	p.Glu630Asp(p.E630D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000297029
Start	12649468:12649468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755211011
CDS Mutation	c.1883T>C
AA Mutation	p.Ile628Thr(p.I628T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000297029
Start	12629168:12629168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750738162
CDS Mutation	c.1265G>A
AA Mutation	p.Gly422Asp(p.G422D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000297029
Start	12622805:12622805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671T>C
AA Mutation	p.Leu224Ser(p.L224S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297029
Start	12625096:12625096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000297029
Start	12644099:12644159(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1582-33_1609delTGAATCATTGTTTTATTTTTCTTCATATTCCAGGTTGATGTTGATGCAAATTCACTGAATT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SCIN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297029
Start	12625776:12625776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907C>T
AA Mutation	p.Pro303Ser(p.P303S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297029
Start	12644176:12644176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1620T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297029
Start	12570871:12570871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85C>T
Mutation Classification	Silent
Feature Type	Transcript