Colon Cancer: Gene >> SRC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358208
Start	37403339:37403339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1571C>T
AA Mutation	p.Thr524Met(p.T524M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358208
Start	37393983:37393983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439C>A
AA Mutation	p.Gln147Lys(p.Q147K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358208
Start	37403257:37403257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1489C>A
AA Mutation	p.Leu497Ile(p.L497I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358208
Start	37402455:37402455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370628677
CDS Mutation	c.1137C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358208
Start	37396196:37396196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140451827
CDS Mutation	c.588C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358208
Start	37402756:37402756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1278A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358208
Start	37396289:37396289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000358208
Start	37386175:37386175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000358208
Start	37384160:37384168(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.12_20delCAAGAGCAA
AA Mutation	p.Asn4_Ser6del(p.N4_S6del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SRC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358208
Start	37402438:37402438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1120G>C
AA Mutation	p.Ala374Pro(p.A374P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript