Colon Cancer: Gene >> TNS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40496257:40496257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147274319
CDS Mutation	c.169G>A
AA Mutation	p.Val57Met(p.V57M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40496155:40496155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>A
AA Mutation	p.Pro91Thr(p.P91T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40480726:40480726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1715C>T
AA Mutation	p.Pro572Leu(p.P572L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40487206:40487206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118C>A
AA Mutation	p.Pro373His(p.P373H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40487168:40487168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1156T>C
AA Mutation	p.Ser386Pro(p.S386P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40496400:40496400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26T>C
AA Mutation	p.Leu9Pro(p.L9P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40488939:40488939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377454691
CDS Mutation	c.470G>T
AA Mutation	p.Arg157Ile(p.R157I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40488886:40488886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523C>T
AA Mutation	p.Pro175Ser(p.P175S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40488638:40488638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771G>T
AA Mutation	p.Glu257Asp(p.E257D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40479747:40479747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1837A>C
AA Mutation	p.Ile613Leu(p.I613L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000254051
Start	40478647:40478647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1912G>T
AA Mutation	p.Val638Leu(p.V638L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TNS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254051
Start	40477601:40477601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2135C>A
AA Mutation	p.Ala712Glu(p.A712E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript