RGD:14719946 Rat Genome Database

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Variant: RGD:14719946 -  Homo sapiens

RGD ID: 14719946
RS ID: rs74469401
ClinVar ID: CV668517
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LITAF  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 11,643,896
GRCh38 16 11,550,040
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009008.1:g.41911C>T
NC_000016.10:g.11550040G>A
NC_000016.9:g.11643896G>A
LRG_253t1:c.*17-295C>T
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LITAF
Accession:NM_001136473
Location:3UTRS;INTRON

Gene Symbol:LITAF
Accession:NM_001136472
Location:INTRON

Gene Symbol:LITAF
Accession:XM_006720983
Location:INTRON

Gene Symbol:LITAF
Accession:XM_006720984
Location:INTRON

Gene Symbol:LITAF
Accession:XM_047434928
Location:INTRON

Gene Symbol:LITAF
Accession:XM_047434929
Location:INTRON

Gene Symbol:LITAF
Accession:XM_047434927
Location:INTRON

Gene Symbol:LITAF
Accession:XM_047434926
Location:INTRON

Gene Symbol:LITAF
Accession:XM_011522754
Location:INTRON

Gene Symbol:LITAF
Accession:XM_006720982
Location:INTRON

Gene Symbol:LITAF
Accession:NM_004862
Location:INTRON

Gene Symbol:LITAF
Accession:NR_024320
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000831003 CLINVAR
dbSNP (RS) rs74469401 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LITAF CLINVAR
OMIM 603795 CLINVAR