RGD:329349514 Rat Genome Database

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Variant: RGD:329349514 -  Homo sapiens

RGD ID: 329349514
ClinVar ID: CV2435300
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BAD  GPR137  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 64,039,217
GRCh38 11 64,271,745
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NP_004313.1:p.Asp82Glu
NP_116784.1:p.Asp82Glu
NM_001378076.1:c.-16+1084G>C
NC_000011.9:g.64039217G>C
More... 		02/16/2023 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:GPR137
Accession:NM_001378078
Location:5UTRS;INTRON

Gene Symbol:GPR137
Accession:NM_001378084
Location:5UTRS;INTRON

Gene Symbol:GPR137
Accession:NM_001378076
Location:5UTRS;INTRON

Gene Symbol:BAD
Accession:NM_032989
Location:EXON
Amino Acid Prediction: D to D (synonymous)
Amino Acid Position: 82
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MFQIPEFEPSEQEDSSSAERGLGPSPAGDGPSGSGKHHRQAPGLLWDASHQQEQPTSSSHHGGAGAVEIRSRHSSYPAGT
EDDEGMGEEPSPFRGRSRSAPPNLWAAQRYGRELRRMSDEFVDSFKKGLPRPKSAGTATQMRQSSSWTRVFQSWWDRNLG
RGSSAPSQ*

Gene Symbol:BAD
Accession:NM_004322
Location:EXON
Amino Acid Prediction: D to D (synonymous)
Amino Acid Position: 82
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MFQIPEFEPSEQEDSSSAERGLGPSPAGDGPSGSGKHHRQAPGLLWDASHQQEQPTSSSHHGGAGAVEIRSRHSSYPAGT
EDDEGMGEEPSPFRGRSRSAPPNLWAAQRYGRELRRMSDEFVDSFKKGLPRPKSAGTATQMRQSSSWTRVFQSWWDRNLG
RGSSAPSQ*

Gene Symbol:GPR137
Accession:NM_001177358
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001170881
Location:INTRON

Gene Symbol:GPR137
Accession:NM_020155
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001170880
Location:INTRON

Gene Symbol:GPR137
Accession:XM_005274102
Location:INTRON

Gene Symbol:GPR137
Accession:XM_005274104
Location:INTRON

Gene Symbol:GPR137
Accession:XM_005274100
Location:INTRON

Gene Symbol:GPR137
Accession:XM_011545168
Location:INTRON

Gene Symbol:GPR137
Accession:XM_011545169
Location:INTRON

Gene Symbol:GPR137
Accession:XM_017018016
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378079
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378083
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378086
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378087
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378081
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378080
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378085
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378077
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378088
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378082
Location:INTRON

Gene Symbol:GPR137
Accession:NM_001378089
Location:INTRON

Gene Symbol:GPR137
Accession:XM_047427264
Location:INTRON

Gene Symbol:GPR137
Accession:XM_047427263
Location:INTRON

Gene Symbol:GPR137
Accession:XM_047427265
Location:INTRON

Gene Symbol:GPR137
Accession:NR_165395
Location:INTRON;NON-CODING

Gene Symbol:GPR137
Accession:NR_165394
Location:INTRON;NON-CODING

Gene Symbol:GPR137
Accession:NR_165397
Location:INTRON;NON-CODING

Gene Symbol:GPR137
Accession:NR_165396
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003179244 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene BAD CLINVAR
  GPR137 CLINVAR
OMIM 603167 CLINVAR