RGD:15120204 Rat Genome Database

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Variant: RGD:15120204 -  Homo sapiens

RGD ID: 15120204
RS ID: rs766038266
ClinVar ID: CV783386
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NFIB  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 14,120,622
GRCh38 9 14,120,623
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001190738.2:c.1140C>T
NM_001282787.2:c.306C>T
NM_001369477.1:c.1005C>T
NM_001369465.1:c.1035C>T
More... 		12/31/2018 non-coding transcript variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NFIB
Accession:NM_001282787
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369474
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369463
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369460
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369467
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369462
Location:EXON

Gene Symbol:NFIB
Accession:NM_001190737
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369468
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369471
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369479
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369480
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369458
Location:EXON

Gene Symbol:NFIB
Accession:NM_005596
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369470
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369473
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369472
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369464
Location:EXON

Gene Symbol:NFIB
Accession:NM_001190738
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369469
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369477
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369478
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369475
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369461
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369476
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369465
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369459
Location:EXON

Gene Symbol:NFIB
Accession:NM_001369466
Location:EXON

Gene Symbol:NFIB
Accession:NR_161382
Location:EXON;NON-CODING

Gene Symbol:NFIB
Accession:NR_161385
Location:EXON;NON-CODING

Gene Symbol:NFIB
Accession:NR_161383
Location:EXON;NON-CODING

Gene Symbol:NFIB
Accession:NR_161384
Location:EXON;NON-CODING

Gene Symbol:NFIB
Accession:NM_001369481
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000979252 CLINVAR
dbSNP (RS) rs766038266 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene NFIB CLINVAR
OMIM 600728 CLINVAR