Colon Cancer: Gene >> CAPN5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77114327:77114327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782492041
CDS Mutation	c.592G>A
AA Mutation	p.Asp198Asn(p.D198N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77119100:77119100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370528920
CDS Mutation	c.1238C>T
AA Mutation	p.Thr413Met(p.T413M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77120735:77120735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782109539
CDS Mutation	c.1313G>A
AA Mutation	p.Arg438His(p.R438H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77115452:77115452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782513405
CDS Mutation	c.757G>A
AA Mutation	p.Ala253Thr(p.A253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77112671:77112671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377123751
CDS Mutation	c.380G>A
AA Mutation	p.Arg127His(p.R127H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77122624:77122624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782766470
CDS Mutation	c.1652C>T
AA Mutation	p.Ser551Leu(p.S551L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77120767:77120767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1345T>A
AA Mutation	p.Ser449Thr(p.S449T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000278559
Start	77120909:77120909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563895448
CDS Mutation	c.1487G>A
AA Mutation	p.Arg496Gln(p.R496Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77119117:77119117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255G>T
AA Mutation	p.Gly419Cys(p.G419C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77123791:77123791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143494790
CDS Mutation	c.1844G>A
AA Mutation	p.Arg615Gln(p.R615Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77114354:77114354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367724731
CDS Mutation	c.619G>A
AA Mutation	p.Asp207Asn(p.D207N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278559
Start	77084985:77084985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141871015
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278559
Start	77084895:77084895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182958020
CDS Mutation	c.9G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278559
Start	77118310:77118310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782714369
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278559
Start	77115457:77115457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199542451
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278559
Start	77115529:77115529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000278559
Start	77122624:77122624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652C>A
AA Mutation	p.Ser551Ter(p.S551*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CAPN5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77123791:77123791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143494790
CDS Mutation	c.1844G>A
AA Mutation	p.Arg615Gln(p.R615Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77120864:77120864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782027905
CDS Mutation	c.1442G>A
AA Mutation	p.Gly481Asp(p.G481D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77123832:77123832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781990034
CDS Mutation	c.1885G>A
AA Mutation	p.Val629Met(p.V629M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77119093:77119093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231C>T
AA Mutation	p.Arg411Trp(p.R411W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278559
Start	77120821:77120821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1399C>T
AA Mutation	p.Arg467Cys(p.R467C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript