Colon Cancer: Gene >> VEPH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157428331:157428331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687A>T
AA Mutation	p.Lys229Asn(p.K229N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157261300:157261300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146047352
CDS Mutation	c.2336G>A
AA Mutation	p.Arg779His(p.R779H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157381289:157381289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.994A>G
AA Mutation	p.Lys332Glu(p.K332E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157495268:157495268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82A>G
AA Mutation	p.Ile28Val(p.I28V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000362010
Start	157313754:157313754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1877G>A
AA Mutation	p.Ser626Asn(p.S626N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157495283:157495283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67T>G
AA Mutation	p.Leu23Val(p.L23V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157428437:157428437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581A>G
AA Mutation	p.Gln194Arg(p.Q194R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157265635:157265635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2156T>C
AA Mutation	p.Ile719Thr(p.I719T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157428326:157428326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692T>A
AA Mutation	p.Leu231His(p.L231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157470476:157470476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192A>C
AA Mutation	p.Arg64Ser(p.R64S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157428382:157428382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636G>T
AA Mutation	p.Gln212His(p.Q212H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157428485:157428485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533A>G
AA Mutation	p.Asn178Ser(p.N178S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157381307:157381307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976A>G
AA Mutation	p.Ile326Val(p.I326V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362010
Start	157261242:157261242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2394C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362010
Start	157428325:157428325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775503594
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000362010
Start	157364318:157364318(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1322delA
AA Mutation	p.Asn441ThrfsTer42(p.N441Tfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000362010
Start	157265579:157265579(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2212delA
AA Mutation	p.Thr738HisfsTer27(p.T738Hfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000362010
Start	157364412:157364412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1228C>T
AA Mutation	p.Gln410Ter(p.Q410*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> VEPH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157286572:157286572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2113C>A
AA Mutation	p.Pro705Thr(p.P705T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362010
Start	157364485:157364485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155C>A
AA Mutation	p.Phe385Leu(p.F385L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript