or
or
Exact

Results for "MYH7B"

Variant Events: 25

Gene
Gene symbol on which the variant is located
ID
Subject Identifier from the original study
Location
Genomic location of the reference allele
REF
Reference allele
ALT
Alternate allele
Context
Variant functional categories
Variant validation performed by an orthogonal method and reported
Inheritance
Reported inheritance status
Effects
Variant effect on transcript per Annovar
Transcript
Transcript used for the cDNA/Protein mutation
cDNA
cDNA variant notation
Protein
Protein variant notation
CADD-Phred v1.0
CADD phred-like score. This is phred-like rank score based on whole genome CADD raw scores
ExAC v0.3
ExAC population frequency (version 0.3)
Sources
Source(s) where variants from this event are reported
MYH7B     200675376@1082034681chr20:
33567509-33567509
CGexonicDe novononsynonymous SNVNM_020884c.C370Gp.R124G16.818.295E-6Satterstrom2020 E
Trost2022 G
Zhou2022 GE
MYH7B     mAGRE2158chr20:
33568838-33568838
CTexonicPaternalstopgainNM_020884c.C628Tp.R210X27.88.281E-6Cirnigliaro2023 G
MYH7B     09C80346chr20:
33578059-33578059
GAexonicDe novosynonymous SNVNM_020884c.G2049Ap.V683V--DeRubeis2014 E
Fu2022 E
Kosmicki2017 E
Lim2017 E
Satterstrom2020 E
Trost2022 G
Zhou2022 GE
MYH7B     5-5040-003chr20:
33570270-33570270
CTexonicDe novononsynonymous SNVNM_020884c.C662Tp.S221L26.18.34E-6Trost2022 G
Zhou2022 GE
MYH7B     200675376_1082034681chr20:
33567509-33567509
CGexonicDe novononsynonymous SNVNM_020884c.C370Gp.R124G16.818.295E-6Fu2022 E
MYH7B     4915chr20:
33581221-33581221
CGexonicDe novononsynonymous SNVNM_020884c.C2518Gp.R840G10.66-Fu2022 E
MYH7B     MSSNG00101-003chr20:
33584549-33584549
AGexonicDe novononsynonymous SNVNM_020884c.A3380Gp.E1127G17.78-Trost2022 G
Zhou2022 GE
MYH7B     mAGRE5320chr20:
33576011-33576011
GAexonicPaternalstopgainNM_020884c.G1659Ap.W553X38.0-Cirnigliaro2023 G
MYH7B     mAGRE1876chr20:
33575451-33575451
CAexonicMaternalstopgainNM_020884c.C1365Ap.Y455X20.93.326E-5Cirnigliaro2023 G
MYH7B     mAGRE1875chr20:
33575451-33575451
CAexonicMaternalstopgainNM_020884c.C1365Ap.Y455X20.93.326E-5Cirnigliaro2023 G
MYH7B     14293.p1chr20:
33575348-33575348
GAintronicDe novo-1.0E-4Iossifov2014 E
Kosmicki2017 E
MYH7B     iHART1876chr20:
33575451-33575451
CAexonicMaternalstopgainNM_020884c.C1365Ap.Y455X20.93.326E-5Ruzzo2019 G
MYH7B     iHART2158chr20:
33568838-33568838
CTexonicPaternalstopgainNM_020884c.C628Tp.R210X27.88.281E-6Ruzzo2019 G
MYH7B     31716chr20:
33588702-33588702
GCintronicDe novo--Trost2022 G
MYH7B     iHART1875chr20:
33575451-33575451
CAexonicMaternalstopgainNM_020884c.C1365Ap.Y455X20.93.326E-5Ruzzo2019 G
MYH7B     REACH000714chr20:
33588185-33588185
ATexonicDe novononsynonymous SNVNM_020884c.A4997Tp.K1666M21.50.0046Trost2022 G
MYH7B     MSSNG00257-003chr20:
33580521-33580521
CTintronicDe novo--Trost2022 G
MYH7B     MSSNG00078-003chr20:
33572123-33572123
CTintronicDe novo--Trost2022 G
MYH7B     5-0050-004chr20:
33569620-33569620
ACintronicDe novo--Trost2022 G
MYH7B     Chen2017:21chr20:
33567509-33567509
CGexonicDe novononsynonymous SNVNM_020884c.C370Gp.R124G16.818.295E-6Chen2017 E
MYH7B     PN400506chr20:
33584197-33584197
CTexonicInheritednonsynonymous SNVNM_020884c.C3118Tp.R1040W20.60.012Leblond2019 E
MYH7B     SP0048375chr20:
33575185-33575185
ACintronicDe novo--Fu2022 E
MYH7B     11749.p1chr20:
33588702-33588702
GCintronicDe novo--Satterstrom2020 E
MYH7B     SP0152806chr20:
33574023-33574023
GAintronicDe novo-8.818E-5Fu2022 E
MYH7B     SP0032113chr20:
33586580-33586580
GAexonicDe novononsynonymous SNVNM_020884c.G4178Ap.R1393Q35.02.598E-5Fu2022 E
Trost2022 G
Zhou2022 GE
Source Variant Information

, -

Source:

Paper alias:

No records found.
Paper Information
Title
Authors
Technology
Variant source
Cohorts
Design
URL
Pubmed
Subject count
The number of subjects for this study could not be determined directly from the variant data; the value given is that reported by the authors in the publication.
Variant event count
Curation notesView
More