Colon Cancer: Gene >> TAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354258
Start	32853116:32853116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572060702
CDS Mutation	c.701G>A
AA Mutation	p.Arg234His(p.R234H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354258
Start	32853366:32853366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451G>A
AA Mutation	p.Gly151Ser(p.G151S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354258
Start	32851075:32851075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099C>A
AA Mutation	p.Leu367Met(p.L367M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354258
Start	32847930:32847930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1909C>A
AA Mutation	p.Leu637Met(p.L637M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000354258
Start	32847515:32847515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2081C>A
AA Mutation	p.Thr694Lys(p.T694K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354258
Start	32851059:32851059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115G>A
AA Mutation	p.Arg372Gln(p.R372Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354258
Start	32853344:32853344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473C>A
AA Mutation	p.Pro158Gln(p.P158Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354258
Start	32848768:32848768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778774698
CDS Mutation	c.1630C>T
AA Mutation	p.Arg544Cys(p.R544C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354258
Start	32853604:32853604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354258
Start	32853757:32853757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354258
Start	32850494:32850494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354258
Start	32847538:32847538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2058T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000354258
Start	32853284:32853284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533C>G
AA Mutation	p.Ser178Ter(p.S178*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000354258
Start	32850436:32850436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143800384
CDS Mutation	c.1312C>T
AA Mutation	p.Arg438Ter(p.R438*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354258
Start	32848674:32848674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760636031
CDS Mutation	c.1724G>A
AA Mutation	p.Arg575His(p.R575H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354258
Start	32852204:32852204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.929A>C
AA Mutation	p.Asn310Thr(p.N310T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000354258
Start	32847627:32847627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1969G>T
AA Mutation	p.Glu657Ter(p.E657*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000354258
Start	32850436:32850436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143800384
CDS Mutation	c.1312C>T
AA Mutation	p.Arg438Ter(p.R438*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript