Colon Cancer: Gene >> MYRF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278836
Start	61770284:61770284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.499T>C
AA Mutation	p.Cys167Arg(p.C167R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278836
Start	61777382:61777382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1709C>T
AA Mutation	p.Ala570Val(p.A570V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278836
Start	61770392:61770392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Trp(p.R203W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278836
Start	61776114:61776114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762223967
CDS Mutation	c.1370G>A
AA Mutation	p.Arg457Gln(p.R457Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278836
Start	61774150:61774150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1299G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278836
Start	61771728:61771728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278836
Start	61776424:61776424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200751113
CDS Mutation	c.1491G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278836
Start	61770352:61770352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278836
Start	61784355:61784355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3270A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278836
Start	61770325:61770325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.540A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278836
Start	61779850:61779850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142542699
CDS Mutation	c.2256C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278836
Start	61774021:61774021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377523845
CDS Mutation	c.1170C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278836
Start	61779550:61779550(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2232delC
AA Mutation	p.Lys745ArgfsTer45(p.K745Rfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278836
Start	61780767:61780767(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2466delG
AA Mutation	p.Ser823ValfsTer22(p.S823Vfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278836
Start	61771541:61771541(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs774654800
CDS Mutation	c.789delC
AA Mutation	p.Ser264AlafsTer8(p.S264Afs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278836
Start	61771540:61771541(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs769274302
CDS Mutation	c.789dupC
AA Mutation	p.Ser264GlnfsTer74(p.S264Qfs*74)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MYRF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278836
Start	61780983:61780983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200193085
CDS Mutation	c.2510C>T
AA Mutation	p.Thr837Met(p.T837M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278836
Start	61774025:61774025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1174G>A
AA Mutation	p.Asp392Asn(p.D392N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript