RGD:401930751 Rat Genome Database

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Variant: RGD:401930751 -  Homo sapiens

RGD ID: 401930751
ClinVar ID: CV2828488
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FER1L6  FER1L6-AS2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 125,094,521
GRCh38 8 124,082,280
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001039112.2:c.4221-8G>C
NC_000008.11:g.124082280G>C
NC_000008.10:g.125094521G>C
 07/01/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FER1L6
Accession:NM_001039112
Location:INTRON

Gene Symbol:FER1L6
Accession:XM_006716618
Location:INTRON

Gene Symbol:FER1L6
Accession:XM_011517231
Location:INTRON

Gene Symbol:FER1L6
Accession:XM_011517235
Location:INTRON

Gene Symbol:FER1L6
Accession:XM_011517232
Location:INTRON

Gene Symbol:FER1L6
Accession:XM_011517233
Location:INTRON

Gene Symbol:FER1L6
Accession:XM_011517236
Location:INTRON

Gene Symbol:FER1L6
Accession:XM_047422118
Location:INTRON

Gene Symbol:FER1L6
Accession:XM_047422117
Location:INTRON

Gene Symbol:FER1L6-AS2
Accession:NR_103547
Location:INTRON;NON-CODING

Gene Symbol:FER1L6
Accession:XR_928347
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003440623 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FER1L6 CLINVAR
  FER1L6-AS2 CLINVAR