Colon Cancer: Gene >> MSH5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375750
Start	31753580:31753580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.965G>A
AA Mutation	p.Arg322His(p.R322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375750
Start	31758202:31758202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1052G>A
AA Mutation	p.Arg351His(p.R351H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375750
Start	31759122:31759122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139002853
CDS Mutation	c.1352G>A
AA Mutation	p.Arg451His(p.R451H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375750
Start	31760768:31760768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1891A>G
AA Mutation	p.Ile631Val(p.I631V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375750
Start	31761945:31761945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2309G>A
AA Mutation	p.Arg770His(p.R770H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375750
Start	31758232:31758232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145281780
CDS Mutation	c.1082G>A
AA Mutation	p.Arg361Gln(p.R361Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375750
Start	31761543:31761543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2109C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375750
Start	31743127:31743127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375750
Start	31762117:31762117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2325A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000375750
Start	31760777:31760777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1900C>T
AA Mutation	p.Arg634Ter(p.R634*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375750
Start	31761495:31761496(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2061_2062insACACA
AA Mutation	p.Ala688ThrfsTer25(p.A688Tfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MSH5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375750
Start	31760705:31760705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1828T>G
AA Mutation	p.Phe610Val(p.F610V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript