Colon Cancer: Gene >> FAP

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000188790
Start	162203143:162203143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1050C>A
AA Mutation	p.Phe350Leu(p.F350L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000188790
Start	162214050:162214050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141855900
CDS Mutation	c.890C>T
AA Mutation	p.Thr297Met(p.T297M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000188790
Start	162188170:162188170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1813A>G
AA Mutation	p.Arg605Gly(p.R605G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000188790
Start	162188253:162188253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1730C>T
AA Mutation	p.Thr577Ile(p.T577I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000188790
Start	162188179:162188179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1804A>G
AA Mutation	p.Thr602Ala(p.T602A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000188790
Start	162183423:162183423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1860A>G
AA Mutation	p.Ile620Met(p.I620M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000188790
Start	162188361:162188361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1622A>G
AA Mutation	p.Tyr541Cys(p.Y541C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000188790
Start	162213972:162213972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.968T>G
AA Mutation	p.Phe323Cys(p.F323C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000188790
Start	162218089:162218089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659T>G
AA Mutation	p.Phe220Cys(p.F220C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000188790
Start	162189699:162189699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506G>T
AA Mutation	p.Gln502His(p.Q502H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000188790
Start	162202875:162202875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220C>T
AA Mutation	p.Ser407Leu(p.S407L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000188790
Start	162218028:162218028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185593943
CDS Mutation	c.720C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000188790
Start	162171060:162171060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138589105
CDS Mutation	c.2202C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000188790
Start	162215963:162215963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747937736
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000188790
Start	162173214:162173214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2042C>A
AA Mutation	p.Thr681Asn(p.T681N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000188790
Start	162203105:162203105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762738740
CDS Mutation	c.1088C>T
AA Mutation	p.Ser363Leu(p.S363L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000188790
Start	162203044:162203044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000188790
Start	162198857:162198857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1302A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000188790
Start	162188261:162188261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1722T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000188790
Start	162198791:162198791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199889478
CDS Mutation	c.1368C>T
Mutation Classification	Silent
Feature Type	Transcript