rs181651384 Rat Genome Database

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Variant: rs181651384 -  Homo sapiens

RGD ID: 11349087
RS ID: rs181651384
ClinVar ID: CV238213
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LEFTY2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 226,127,623
GRCh38 1 225,939,923
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008118.1:g.6298C>T
NC_000001.11:g.225939923G>A
NC_000001.10:g.226127623G>A
NP_003231.2:p.Asn110=
More...
12/21/2023 intron variant benign|likely benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LEFTY2
Accession:NM_003240
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 110
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MWPLWLCWALWVLPLAGPGAALTEEQLLGSLLRQLQLSEVPVLDRADMEKLVIPAHVRAQYVVLLRRSHGDRSRGKRFSQ
SFREVAGRFLASEASTHLLVFGMEQRLPPNSELVQAVLRLFQEPVPKAALHRHGRLSPRSAQARVTVEWLRVRDDGSNRT
SLIDSRLVSVHESGWKAFDVTEAVNFWQQLSRPRQPLLLQVSVQREHLGPLASGAHKLVRFASQGAPAGLGEPQLELHTL
DLRDYGAQGDCDPEAPMTEGTRCCRQEMYIDLQGMKWAKNWVLEPPGFLAYECVGTCQQPPEALAFNWPFLGPRQCIASE
TASLPMIVSIKEGGRTRPQVVSLPNMRVQKCSCASDGALVPRRLQP*

Gene Symbol:LEFTY2
Accession:XM_011544266
Location:EXON
Amino Acid Prediction: N to N (synonymous)
Amino Acid Position: 110
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MWPLWLCWALWVLPLAGPGAALTEEQLLGSLLRQLQLSEVPVLDRADMEKLVIPAHVRAQYVVLLRRSHGDRSRGKRFSQ
SFREVAGRFLASEASTHLLVFGMEQRLPPNSELVQAVLRLFQEPVPKAALHRHGRLSPRSAQARVTVEWLRVRDDGSNRT
SLIDSRLVSVHESGWKAFDVTEAVNFWQQLSRPRQPLLLQVSVQREHLGPLASGAHKLVRFASQGAPAGLGEPQLELHTL
DLRDYGYVYSSSHKYPAFRT*

Gene Symbol:LEFTY2
Accession:NM_001172425
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000229178 CLINVAR
  RCV004713421 CLINVAR
dbSNP (RS) rs181651384 CLINVAR
MedGen C1866091 CLINVAR
  C3661900 CLINVAR
NCBI Gene LEFTY2 CLINVAR
OMIM 601877 CLINVAR