RGD:151232399 Rat Genome Database

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Variant: RGD:151232399 -  Homo sapiens

RGD ID: 151232399
RS ID: rs147475536
ClinVar ID: CV1316770
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MTRR  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 7,875,337
GRCh38 5 7,875,224
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002454.3:c.284-34T>C
NM_024010.4:c.284-34T>C
NG_008856.1:g.11121T>C
NM_001364440.2:c.284-34T>C
More... 		05/26/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MTRR
Accession:NM_002454
Location:INTRON

Gene Symbol:MTRR
Accession:NM_024010
Location:INTRON

Gene Symbol:MTRR
Accession:XM_024446064
Location:INTRON

Gene Symbol:MTRR
Accession:NM_001364440
Location:INTRON

Gene Symbol:MTRR
Accession:NM_001364441
Location:INTRON

Gene Symbol:MTRR
Accession:NM_001364442
Location:INTRON

Gene Symbol:MTRR
Accession:XM_047417233
Location:INTRON

Gene Symbol:MTRR
Accession:XM_047417234
Location:INTRON

Gene Symbol:MTRR
Accession:XM_047417235
Location:INTRON

Gene Symbol:MTRR
Accession:XM_047417236
Location:INTRON

Gene Symbol:MTRR
Accession:XM_047417237
Location:INTRON

Gene Symbol:MTRR
Accession:XM_047417238
Location:INTRON

Gene Symbol:MTRR
Accession:NR_134481
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_134480
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_134482
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157176
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157178
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157175
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157177
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157170
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157174
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157172
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157173
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157168
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157171
Location:INTRON;NON-CODING

Gene Symbol:MTRR
Accession:NR_157169
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001786590 CLINVAR
dbSNP (RS) rs147475536 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MTRR CLINVAR
OMIM 602568 CLINVAR