RGD:11589395 Rat Genome Database

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Variant: RGD:11589395 -  Homo sapiens

RGD ID: 11589395
ClinVar ID: CV300666
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MEF2C  MEF2C-AS2  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 88,017,084
GRCh38 5 88,721,267
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001131005.2:c.*1337A>T
NG_023427.1:g.187839A>T
NC_000005.10:g.88721267T>A
NC_000005.9:g.88017084T>A
More...
06/14/2016 3 prime utr variant uncertain significance

Variant Details
Variant Transcripts
Gene Symbol:MEF2C
Accession:NM_001131005
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001193347
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001193350
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_002397
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001193348
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001193349
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_005248511
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_011543396
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001308002
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_017009478
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_024446055
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_024446058
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_024446059
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_024446056
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364329
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364330
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364333
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364344
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364331
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364353
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364345
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364354
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364352
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364349
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364347
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364355
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364348
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364346
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364334
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364335
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364332
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364343
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364338
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364339
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364337
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364340
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364336
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364342
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364341
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364350
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364357
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001364356
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:NM_001363581
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417190
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417181
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417202
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417191
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417182
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417196
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417203
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417192
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417194
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417188
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417217
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417201
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417185
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417193
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417195
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417199
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417186
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417189
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417197
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417183
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417187
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417198
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417184
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417200
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417208
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417213
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417206
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417204
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417214
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417207
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417205
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417210
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417216
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417211
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417209
Location:3UTRS;EXON

Gene Symbol:MEF2C
Accession:XM_047417215
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:MEF2C-AS2
Accession:NR_146284
Location:INTRON;NON-CODING

Variant Samples