Mutation

Primary Site >> Liver Cancer

Gene >> MYH7

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355349
Start	23424820:23424820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2628G>C
AA Mutation	p.Lys876Asn(p.K876N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355349
Start	23416096:23416096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4861G>T
AA Mutation	p.Asp1621Tyr(p.D1621Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355349
Start	23431771:23431771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629G>A
AA Mutation	p.Ser210Asn(p.S210N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355349
Start	23432485:23432485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524T>G
AA Mutation	p.Leu175Arg(p.L175R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355349
Start	23433178:23433178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251T>C
AA Mutation	p.Phe84Ser(p.F84S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355349
Start	23433133:23433133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296C>T
AA Mutation	p.Pro99Leu(p.P99L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355349
Start	23429255:23429255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs730880868
CDS Mutation	c.1231G>A
AA Mutation	p.Val411Ile(p.V411I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355349
Start	23425977:23425977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2149G>T
AA Mutation	p.Asp717Tyr(p.D717Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355349
Start	23414008:23414008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5654C>T
AA Mutation	p.Ala1885Val(p.A1885V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355349
Start	23415101:23415101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5453G>C
AA Mutation	p.Arg1818Pro(p.R1818P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355349
Start	23432712:23432712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355349
Start	23415079:23415079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5475G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355349
Start	23423670:23423670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2976G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355349
Start	23420042:23420042(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3529delG
AA Mutation	p.Asp1177ThrfsTer37(p.D1177Tfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript