RGD:401916450 Rat Genome Database

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Variant: RGD:401916450 -  Homo sapiens

RGD ID: 401916450
ClinVar ID: CV2814427
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BNC1  LOC105370932  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 83,953,339
GRCh38 15 83,284,587
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001717.4:c.42C>T
NG_131960.1:g.633G>A
NC_000015.10:g.83284587G>A
NC_000015.9:g.83953339G>A
More... 		02/01/2024 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:BNC1
Accession:NM_001717
Location:EXON
Amino Acid Prediction: A to A (synonymous)
Amino Acid Position: 14
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MRRRPPSRGGRGAARARETRRQPRHRSGRRMAEAISCTLNCSCQSFKPGKINHRQCDQCKHGWVAHALSKLRIPPMYPTS
QVEIVQSNVVFDISSLMLYGTQAIPVRLKILLDRLFSVLKQDEVLQILHALDWTLQDYIRGYVLQDASGKVLDHWSIMTS
EEEVATLQQFLRFGETKSIVELMAIQEKEEQSIIIPPSTANVDIRAFIESCSHRSSSLPTPVDKGNPSSIHPFENLISNM
TFMLPFQFFNPLPPALIGSLPEQYMLEQGHDQSQDPKQEVHGPFPDSSFLTSSSTPFQVEKDQCLNCPDAITKKEDSTHL
SDSSSYNIVTKFERTQLSPEAKVKPERNSLGTKKGRVFCTACEKTFYDKGTLKIHYNAVHLKIKHKCTIEGCNMVFSSLR
SRNRHSANPNPRLHMPMNRNNRDKDLRNSLNLASSENYKCPGFTVTSPDCRPPPSYPGSGEDSKGQPAFPNIGQNGVLFP
NLKTVQPVLPFYRSPATPAEVANTPGILPSLPLLSSSIPEQLISNEMPFDALPKKKSRKSSMPIKIEKEAVEIANEKRHN
LSSDEDMPLQVVSEDEQEACSPQSHRVSEEQHVQSGGLGKPFPEGERPCHRESVIESSGAISQTPEQATHNSERETEQTP
ALIMVPREVEDGGHEHYFTPGMEPQVPFSDYMELQQRLLAGGLFSALSNRGMAFPCLEDSKELEHVGQHALARQIEENRF
QCDICKKTFKNACSVKIHHKNMHVKEMHTCTVEGCNATFPSRRSRDRHSSNLNLHQKALSQEALESSEDHFRAAYLLKDV
AKEAYQDVAFTQQASQTSVIFKGTSRMGSLVYPITQVHSASLESYNSGPLSEGTILDLSTTSSMKSESSSHSSWDSDGVS
EEGTVLMEDSDGNCEGSSLVPGEDEYPICVLMEKADQSLASLPSGLPITCHLCQKTYSNKGTFRAHYKTVHLRQLHKCKV
PGCNTMFSSVRSRNRHSQNPNLHKSLASSPSHLQ*

Gene Symbol:BNC1
Accession:NM_001301206
Location:INTRON

Gene Symbol:BNC1
Accession:XM_011521893
Location:INTRON

Gene Symbol:BNC1
Accession:XM_011521894
Location:INTRON

Gene Symbol:LOC105370932
Accession:XR_932541
Location:INTRON;NON-CODING

Gene Symbol:LOC105370932
Accession:XR_932542
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003400991 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BNC1 CLINVAR
OMIM 601930 CLINVAR