RGD:155976177 Rat Genome Database

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Variant: RGD:155976177 -  Homo sapiens

RGD ID: 155976177
ClinVar ID: CV2342743
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FNDC7  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 109,265,160
GRCh38 1 108,722,538
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001144937.3:c.802G>A
NC_000001.11:g.108722538G>A
NC_000001.10:g.109265160G>A
NM_001144937.1:c.802G>A
More... 		08/30/2021 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:FNDC7
Accession:NM_001144937
Location:EXON
Amino Acid Prediction: A to T (nonsynonymous)
Amino Acid Position: 268
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAGGRETCLPLIGFILICLKMVASAKSAPEIPTIDQAYSKLSNSITVEWATVPGATSYLLTAEDGDTVIETTVANSPGTV
TGLKAATWYEITIRSISAAGRSQASPPKQAKTVLAAPILEVSSPSSDSILVQWEAVYMAIAFSVSIMRANGLGSIWKENT
TNTSLTFTSLEAGTLYTIKAYAWNANRIPGDDSTCNQRTSPRAPANIQVSFDSGALKASFSWARAEGAFNYTVMALSDSS
ELTCSTTFSSCTISSLQCGTEYLISVLTSNDAGSSKSSSAMTLKTVACAPGRVTIQEDPPGHLSVAWSSVDLGDYYVVFV
KSDDGLEVHCNTSLTQCNFLSECGFTYFISVFVYNKAGQSPLGDIFNYTTAPCCPSDINPVLVSSDRVEIVWSPVRGAEL
YETKAVDGYNMVECNDTTPACTLSALECDTKYNITVYSFNEVRGSNMSCTPQFITTAPCSPEIKNVSRDAFSMINVHWRS
TNDDATYTVTAQGEKGLYQCSSTGESCTMRGLPCGSVFSVTAVAETQAGRSLPSYSVPLETVPCCPTGLTVTQITQSVIN
VSWTIGRVAQTHVAVLESHTGQSKCHTHQNHCLLGCITCGINYTVTLKAISATGLTADCSYQSYFSGACCPLGVKLYRLG
PNGIRIYWQASRGSANYSTDLYGSKGIFTCTPSAGLSFCDVTEIPCGDVYTVMVSPVAKTGLKLTFCPKKIYSVTCSGST
LGMVIYRGKRNEE*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004189788 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene FNDC7 CLINVAR
  LOC129931080 CLINVAR