RGD:401921372 Rat Genome Database

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Variant: RGD:401921372 -  Homo sapiens

RGD ID: 401921372
ClinVar ID: CV2826797
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SERTM2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 110,762,097
GRCh38 X 111,518,869
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001354473.2:c.12G>A
NC_000023.11:g.111518869G>A
NC_000023.10:g.110762097G>A
NR_033974.1:n.1065G>A
More... 		04/01/2023 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SERTM2
Accession:NM_001354473
Location:EXON
Amino Acid Prediction: A to A (synonymous)
Amino Acid Position: 4
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MMEAHFKYHGNLTGRAHFPTLATEVDTSSDKYSNLYMYVGLFLSLLAILLILLFTMLLRLKHVISPINSDSTESVPQFTD
VEMQSRIPTP*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003432384 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SERTM2 CLINVAR