rs104895538 Rat Genome Database

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Variant: rs104895538 -  Homo sapiens

RGD ID: 8644288
RS ID: rs104895538
ClinVar ID: CV103636
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NCR1  NLRP7  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 55,448,517
GRCh38 19 54,937,149
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NC_000019.10:g.54937149C>T
NC_000019.9:g.55448517C>T
NG_008056.2:g.34095G>A
NG_008056.1:g.15357G>A
More... 		intron variant not provided adulthood 1 in every 600-1000 pregnancies in western countries Gestational trophoblastic neoplasia

Variant Details
Variant Transcripts
Gene Symbol:NCR1
Accession:XM_047439727
Location:INTRON

Gene Symbol:NLRP7
Accession:NM_206828
Location:INTRON

Gene Symbol:NLRP7
Accession:NM_001127255
Location:INTRON

Gene Symbol:NCR1
Accession:NM_001242356
Location:INTRON

Gene Symbol:NLRP7
Accession:NM_001405531
Location:INTRON

Gene Symbol:NCR1
Accession:NM_004829
Location:INTRON

Gene Symbol:NCR1
Accession:NM_001242357
Location:INTRON

Gene Symbol:NCR1
Accession:NM_001145458
Location:INTRON

Gene Symbol:NLRP7
Accession:NM_139176
Location:INTRON

Gene Symbol:NLRP7
Accession:XM_047438386
Location:INTRON

Gene Symbol:NCR1
Accession:NM_001145457
Location:INTRON

Gene Symbol:NCR1
Accession:XM_011527529
Location:INTRON

Gene Symbol:NCR1
Accession:XM_011527530
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000083997 CLINVAR
dbSNP (RS) rs104895538 CLINVAR
MedGen C3463897 CLINVAR
NCBI Gene NCR1 CLINVAR
  NLRP7 CLINVAR
OMIM 231090 CLINVAR
  604530 CLINVAR
  609661 CLINVAR