Colon Cancer: Gene >> PELP1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000574876
Start	4690991:4690991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317T>C
AA Mutation	p.Phe106Ser(p.F106S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4672457:4672457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753210674
CDS Mutation	c.2534C>T
AA Mutation	p.Pro845Leu(p.P845L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4671877:4671877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775710694
CDS Mutation	c.3114G>C
AA Mutation	p.Glu1038Asp(p.E1038D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4682847:4682847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526C>A
AA Mutation	p.His176Asn(p.H176N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4672775:4672775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2216T>C
AA Mutation	p.Ile739Thr(p.I739T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4672988:4672988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766876710
CDS Mutation	c.2003C>T
AA Mutation	p.Pro668Leu(p.P668L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4672261:4672261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2730T>A
AA Mutation	p.Phe910Leu(p.F910L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4676424:4676424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786G>T
AA Mutation	p.Gln262His(p.Q262H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4672177:4672177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2814A>T
AA Mutation	p.Glu938Asp(p.E938D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4672953:4672953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2038G>C
AA Mutation	p.Ala680Pro(p.A680P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4674614:4674614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1478C>T
AA Mutation	p.Ala493Val(p.A493V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4672601:4672601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2390C>T
AA Mutation	p.Pro797Leu(p.P797L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4676081:4676081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373744745
CDS Mutation	c.935G>A
AA Mutation	p.Arg312Gln(p.R312Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4674948:4674948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283G>A
AA Mutation	p.Arg428Gln(p.R428Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4673383:4673383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750151202
CDS Mutation	c.1712C>T
AA Mutation	p.Thr571Met(p.T571M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574876
Start	4672756:4672756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2235T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574876
Start	4673017:4673017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750844787
CDS Mutation	c.1974G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574876
Start	4673014:4673014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1977C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574876
Start	4675357:4675357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574876
Start	4672150:4672150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112480622
CDS Mutation	c.2841A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574876
Start	4676068:4676068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781244089
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574876
Start	4672615:4672615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116554252
CDS Mutation	c.2376C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000574876
Start	4672033:4672033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2958G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000574876
Start	4690923:4690924(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.384_385insTC
AA Mutation	p.Val129SerfsTer28(p.V129Sfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PELP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000574876
Start	4673366:4673366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767650542
CDS Mutation	c.1729C>T
AA Mutation	p.Arg577Cys(p.R577C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript