Colon Cancer: Gene >> CRYBB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215939
Start	26612096:26612096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750427170
CDS Mutation	c.275G>A
AA Mutation	p.Arg92His(p.R92H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215939
Start	26616291:26616291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776964678
CDS Mutation	c.29C>T
AA Mutation	p.Ser10Leu(p.S10L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215939
Start	26607990:26607990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.331G>A
AA Mutation	p.Gly111Arg(p.G111R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000215939
Start	26612141:26612141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759541633
CDS Mutation	c.230C>T
AA Mutation	p.Ser77Leu(p.S77L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000215939
Start	26601879:26601879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370395737
CDS Mutation	c.575C>T
AA Mutation	p.Thr192Ile(p.T192I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000215939
Start	26602004:26602004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450A>C
AA Mutation	p.Lys150Asn(p.K150N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215939
Start	26607898:26607898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000215939
Start	26616243:26616244(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.76dupG
AA Mutation	p.Ala26GlyfsTer9(p.A26Gfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CRYBB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215939
Start	26612153:26612153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775211493
CDS Mutation	c.218G>A
AA Mutation	p.Arg73Gln(p.R73Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215939
Start	26612156:26612156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767583919
CDS Mutation	c.215G>A
AA Mutation	p.Arg72His(p.R72H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215939
Start	26607992:26607992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533532537
CDS Mutation	c.329G>A
AA Mutation	p.Arg110His(p.R110H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000215939
Start	26612178:26612178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193G>A
AA Mutation	p.Glu65Lys(p.E65K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript