Colon Cancer: Gene >> TYRO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263798
Start	41568905:41568905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1135G>A
AA Mutation	p.Ala379Thr(p.A379T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263798
Start	41577984:41577984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2381C>T
AA Mutation	p.Ser794Phe(p.S794F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263798
Start	41567492:41567492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.916C>T
AA Mutation	p.Pro306Ser(p.P306S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263798
Start	41573345:41573345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116540200
CDS Mutation	c.2023G>A
AA Mutation	p.Gly675Arg(p.G675R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263798
Start	41568883:41568883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1113G>T
AA Mutation	p.Glu371Asp(p.E371D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263798
Start	41570129:41570129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760003502
CDS Mutation	c.1355G>A
AA Mutation	p.Arg452Gln(p.R452Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263798
Start	41573359:41573359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2037G>T
AA Mutation	p.Lys679Asn(p.K679N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263798
Start	41562624:41562624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263798
Start	41573684:41573684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769707482
CDS Mutation	c.2151G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263798
Start	41577943:41577943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2340T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263798
Start	41561563:41561563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56017003
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263798
Start	41573383:41573383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2061T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263798
Start	41570265:41570265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1408C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263798
Start	41568314:41568314(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1063delC
AA Mutation	p.Leu355TrpfsTer18(p.L355Wfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000263798
Start	41577950:41577950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2347C>T
AA Mutation	p.Arg783Ter(p.R783*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TYRO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263798
Start	41568944:41568944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375597382
CDS Mutation	c.1174G>A
AA Mutation	p.Val392Ile(p.V392I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263798
Start	41561257:41561257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255C>A
AA Mutation	p.Asn85Lys(p.N85K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263798
Start	41573742:41573742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758559401
CDS Mutation	c.2209G>A
AA Mutation	p.Glu737Lys(p.E737K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript