Colon Cancer: Gene >> CALCR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359558
Start	93426522:93426522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1361G>A
AA Mutation	p.Arg454His(p.R454H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359558
Start	93443715:93443715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793G>C
AA Mutation	p.Ala265Pro(p.A265P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359558
Start	93426420:93426420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1463A>G
AA Mutation	p.Asn488Ser(p.N488S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359558
Start	93426423:93426423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1460A>G
AA Mutation	p.Asn487Ser(p.N487S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359558
Start	93426523:93426523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1360C>T
AA Mutation	p.Arg454Cys(p.R454C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359558
Start	93436016:93436016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1187G>A
AA Mutation	p.Arg396Lys(p.R396K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359558
Start	93479435:93479435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544410123
CDS Mutation	c.178G>A
AA Mutation	p.Val60Ile(p.V60I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359558
Start	93477666:93477666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.262C>T
AA Mutation	p.Pro88Ser(p.P88S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359558
Start	93479484:93479484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359558
Start	93434268:93434268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1278C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359558
Start	93438263:93438263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761725398
CDS Mutation	c.912G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000359558
Start	93479426:93479426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762940513
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Ter(p.R63*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CALCR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359558
Start	93460885:93460885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686C>A
AA Mutation	p.Ser229Tyr(p.S229Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359558
Start	93479492:93479492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121C>A
AA Mutation	p.Leu41Ile(p.L41I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359558
Start	93436135:93436135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359558
Start	93426482:93426482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000359558
Start	93486986:93486986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50C>G
AA Mutation	p.Ser17Ter(p.S17*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000359558
Start	93477637:93477639(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.289_291delTGG
AA Mutation	p.Trp97del(p.W97del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript