RGD:8626697 Rat Genome Database

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Variant: RGD:8626697 -  Homo sapiens

RGD ID: 8626697
ClinVar ID: CV81841
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IFNA21  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 21,166,158
GRCh38 9 21,166,159
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002175.2:c.454C>T
NG_030029.1:g.5502C>T
NC_000009.12:g.21166159G>A
NC_000009.11:g.21166158G>A
More... 		missense|missense variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:IFNA21
Accession:NM_002175
Location:EXON
Amino Acid Prediction: L to F (nonsynonymous)
Amino Acid Position: 152
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MALSFSLLMAVLVLSYKSICSLGCDLPQTHSLGNRRALILLAQMGRISPFSCLKDRHDFGFPQEEFDGNQFQKAQAISVL
HEMIQQTFNLFSTKDSSATWEQSLLEKFSTELNQQLNDLEACVIQEVGVEETPLMNVDSILAVKKYFQRITFYLTEKKYS
PCAWEVVRAEIMRSFSLSKIFQERLRRKE*
Variant Samples