RGD:8630546 Rat Genome Database

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Variant: RGD:8630546 -  Homo sapiens

RGD ID: 8630546
ClinVar ID: CV85701
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GAP43  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 115,395,162
GRCh38 3 115,676,315
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002045.3:c.333G>A
NM_001130064.1:c.441G>A
NC_000003.12:g.115676315G>A
NC_000003.11:g.115395162G>A
More... 		synonymous variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:GAP43
Accession:NM_002045
Location:EXON
Amino Acid Prediction: E to E (synonymous)
Amino Acid Position: 111
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MLCCMRRTKQVEKNDDDQKIEQDGIKPEDKAHKAATKIQASFRGHITRKKLKGEKKDDVQAAEAEANKKDEAPVADGVEK
KGEGTTTAEAAPATGSKPDEPGKAGETPSEEKKGEGDAATEQAAPQAPASSEEKAGSAETESATKASTDNSPSSKAEDAP
AKEEPKQADVPAAVTAAAATTPAAEDAAAKATAQPPTETGESSQAEENIEAVDETKPKESARQDEGKEEEPEADQEHA*

Gene Symbol:GAP43
Accession:NM_001130064
Location:EXON
Amino Acid Prediction: E to E (synonymous)
Amino Acid Position: 147
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MTKSCSELCHPALHFLPCLGGLRKNLQRAVRPSPYSLGFLTFWISRVEKNDDDQKIEQDGIKPEDKAHKAATKIQASFRG
HITRKKLKGEKKDDVQAAEAEANKKDEAPVADGVEKKGEGTTTAEAAPATGSKPDEPGKAGETPSEEKKGEGDAATEQAA
PQAPASSEEKAGSAETESATKASTDNSPSSKAEDAPAKEEPKQADVPAAVTAAAATTPAAEDAAAKATAQPPTETGESSQ
AEENIEAVDETKPKESARQDEGKEEEPEADQEHA*
Variant Samples