RGD:401922099 Rat Genome Database

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Variant: RGD:401922099 -  Homo sapiens

RGD ID: 401922099
ClinVar ID: CV2819895
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC107303342  TATDN2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 10,312,075
GRCh38 3 10,270,391
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_014760.4:c.1209C>T
NG_046758.1:g.16909C>T
NC_000003.12:g.10270391C>T
NC_000003.11:g.10312075C>T
More... 		03/01/2022 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TATDN2
Accession:NM_014760
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 403
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MASERGKVKHNWSSTSEGCPRKRSCLREPCDVAPSSRPAQRSASRSGGPSSPKRLKAQKEDDVACSRRLSWGSSRRRNNS
SSSFSPHFLGPGVGGAASKGCLIRNTRGFLSSGGSPLRPANASLEEMASLEEEACSLKVDSKDSSHNSTNSEFAAEAEGQ
NDTIEEPNKVQKRKRDRLRDQGSTMIYLKAIQGILGKSMPKRKGEAATRAKPSAAEHPSHGEGPARSEGPAKTAEGAARS
VTVTAAQKEKDATPEVSMEEDKTVPERSSFYDRRVVIDPQEKPSEEPLGDRRTVIDKCSPPLEFLDDSDSHLEIQKHKDR
EVVMEHPSSGSDWSDVEEISTVRFSQEEPVSLKPSAVPEPSSFTTDYVMYPPHLYSSPWCDYASYWTSSPKPSSYPSTGS
SSNDAAQVGKSSRSRMSDYSPNSTGSVQNTSRDMEASEEGWSQNSRSFRFSRSSEEREVKEKRTFQEEMPPRPCGGHASS
SLPKSHLEPSLEEGFIDTHCHLDMLYSKLSFQGTFTKFRKIYSSSFPKEFQGCISDFCDPRTLTDCLWEELLKEDLVWGA
FGCHPHFARYYSESQERNLLQALRHPKAVAFGEMGLDYSYKCTTPVPEQHKVFERQLQLAVSLKKPLVIHCREADEDLLE
IMKKFVPPDYKIHRHCFTGSYPVIEPLLKYFPNMSVGFTAVLTYSSAWEAREALRQIPLERIIVETDAPYFLPRQVPKSL
CQYAHPGLALHTVREIARVKDQPLSLTLAALRENTSRLYSL*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003433424 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC107303342 CLINVAR
  TATDN2 CLINVAR
OMIM 619330 CLINVAR