RGD:14733685 Rat Genome Database

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Variant: RGD:14733685 -  Homo sapiens

RGD ID: 14733685
RS ID: rs45596931
ClinVar ID: CV661370
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MEF2C  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 88,024,199
GRCh38 5 88,728,382
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001364343.2:c.1070+111T>C
NM_001364335.2:c.1100+111T>C
NM_001364336.2:c.1100+111T>C
NM_001364352.2:c.1070+111T>C
More... 		06/19/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MEF2C
Accession:NM_001364333
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364336
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417203
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_011543396
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417191
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417198
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364334
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001193349
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417181
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417206
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001131005
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_024446055
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_024446059
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364340
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364342
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364356
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417210
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417202
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417185
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001193347
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_005248511
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_024446056
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364330
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417189
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417208
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417211
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417215
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417182
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417196
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_002397
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364339
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417190
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417197
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417183
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001193348
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364344
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364347
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417217
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417186
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417200
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417213
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417188
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364355
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364343
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417187
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417207
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364357
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001363581
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_024446058
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364338
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364354
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364349
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364329
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364332
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001193350
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417193
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417199
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417204
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364348
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417195
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001308002
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_017009478
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364337
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417194
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417184
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364331
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364341
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364345
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364352
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417201
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417205
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417216
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364335
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417192
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364346
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364350
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417209
Location:INTRON

Gene Symbol:MEF2C
Accession:NM_001364353
Location:INTRON

Gene Symbol:MEF2C
Accession:XM_047417214
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000837207 CLINVAR
dbSNP (RS) rs45596931 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MEF2C CLINVAR
OMIM 600662 CLINVAR