Colon Cancer: Gene >> SLC26A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395550
Start	48631116:48631116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1011C>A
AA Mutation	p.Asn337Lys(p.N337K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395550
Start	48632977:48632977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765049864
CDS Mutation	c.430G>A
AA Mutation	p.Val144Met(p.V144M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395550
Start	48629649:48629649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1592A>G
AA Mutation	p.Tyr531Cys(p.Y531C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395550
Start	48627966:48627966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1873G>A
AA Mutation	p.Val625Ile(p.V625I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395550
Start	48633050:48633050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2276849
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395550
Start	48629955:48629955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1446G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395550
Start	48631297:48631297(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.913delG
AA Mutation	p.Ala305ProfsTer10(p.A305Pfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395550
Start	48628696:48628696(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1618delG
AA Mutation	p.Val540Ter(p.V540*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC26A6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395550
Start	48630688:48630688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1167C>T
Mutation Classification	Silent
Feature Type	Transcript