RGD:15142085 Rat Genome Database

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Variant: RGD:15142085 -  Homo sapiens

RGD ID: 15142085
RS ID: rs1396654531
ClinVar ID: CV694883
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NDP  NDP-AS1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 43,817,877
GRCh38 X 43,958,631
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000266.4:c.15A>G
NG_009832.1:g.20045A>G
NC_000023.11:g.43958631T>C
NC_000023.10:g.43817877T>C
More... 		09/21/2018 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NDP
Accession:NM_000266
Location:EXON
Amino Acid Prediction: V to V (synonymous)
Amino Acid Position: 5
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MRKHVLAASFSMLSLLVIMGDTDSKTDSSFIMDSDPRRCMRHHYVDSISHPLYKCSSKMVLLARCEGHCSQASRSEPLVS
FSTVLKQPFRSSCHCCRPQTSKLKALRLRCSGGMRLTATYRYILSCHCEECNS*

Gene Symbol:NDP-AS1
Accession:NR_046631
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000877796 CLINVAR
dbSNP (RS) rs1396654531 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene NDP CLINVAR
  NDP-AS1 CLINVAR
OMIM 300658 CLINVAR