RGD:401741895 Rat Genome Database

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Variant: RGD:401741895 -  Homo sapiens

RGD ID: 401741895
ClinVar ID: CV2697652
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATF3  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 212,792,854
GRCh38 1 212,619,512
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001030287.4:c.503A>T
NM_001674.4:c.503A>T
NG_029871.1:g.59158A>T
NC_000001.11:g.212619512A>T
More... 		06/12/2023 3 prime utr variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:ATF3
Accession:NM_001040619
Location:3UTRS;EXON

Gene Symbol:ATF3
Accession:NM_001206486
Location:3UTRS;EXON

Gene Symbol:ATF3
Accession:NM_001030287
Location:EXON
Amino Acid Prediction: N to I (nonsynonymous)
Amino Acid Position: 168
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MMLQHPGQVSASEVSASAIVPCLSPPGSLVFEDFANLTPFVKEELRFAIQNKHLCHRMSSALESVTVSDRPLGVSITKAE
VAPEEDERKKRRRERNKIAAAKCRNKKKEKTECLQKESEKLESVNAELKAQIEELKNEKQHLIYMLNLHRPTCIVRAQNG
RTPEDERILFIQQIKEGTLQS*

Gene Symbol:ATF3
Accession:NM_001206484
Location:EXON
Amino Acid Prediction: N to I (nonsynonymous)
Amino Acid Position: 111
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MSSALESVTVSDRPLGVSITKAEVAPEEDERKKRRRERNKIAAAKCRNKKKEKTECLQKESEKLESVNAELKAQIEELKN
EKQHLIYMLNLHRPTCIVRAQNGRTPEDERILFIQQIKEGTLQS*

Gene Symbol:ATF3
Accession:NM_001674
Location:EXON
Amino Acid Prediction: N to I (nonsynonymous)
Amino Acid Position: 168
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MMLQHPGQVSASEVSASAIVPCLSPPGSLVFEDFANLTPFVKEELRFAIQNKHLCHRMSSALESVTVSDRPLGVSITKAE
VAPEEDERKKRRRERNKIAAAKCRNKKKEKTECLQKESEKLESVNAELKAQIEELKNEKQHLIYMLNLHRPTCIVRAQNG
RTPEDERILFIQQIKEGTLQS*

Gene Symbol:ATF3
Accession:NM_001206488
Location:EXON
Amino Acid Prediction: N to I (nonsynonymous)
Amino Acid Position: 111
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MSSALESVTVSDRPLGVSITKAEVAPEEDERKKRRRERNKIAAAKCRNKKKEKTECLQKESEKLESVNAELKAQIEELKN
EKQHLIYMLNLHRPTCIVRAQNGRTPEDERILFIQQIKEGTLQS*

Gene Symbol:ATF3
Accession:XM_005273146
Location:EXON
Amino Acid Prediction: N to I (nonsynonymous)
Amino Acid Position: 168
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MMLQHPGQVSASEVSASAIVPCLSPPGSLVFEDFANLTPFVKEELRFAIQNKHLCHRMSSALESVTVSDRPLGVSITKAE
VAPEEDERKKRRRERNKIAAAKCRNKKKEKTECLQKESEKLESVNAELKAQIEELKNEKQHLIYMLNLHRPTCIVRAQNG
RTPEDERILFIQQIKEGTLQS*

Gene Symbol:ATF3
Accession:XM_011509579
Location:EXON
Amino Acid Prediction: N to I (nonsynonymous)
Amino Acid Position: 168
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MMLQHPGQVSASEVSASAIVPCLSPPGSLVFEDFANLTPFVKEELRFAIQNKHLCHRMSSALESVTVSDRPLGVSITKAE
VAPEEDERKKRRRERNKIAAAKCRNKKKEKTECLQKESEKLESVNAELKAQIEELKNEKQHLIYMLNLHRPTCIVRAQNG
RTPEDERILFIQQIKEGTLQS*

Gene Symbol:ATF3
Accession:XM_047421211
Location:EXON
Amino Acid Prediction: N to I (nonsynonymous)
Amino Acid Position: 109
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MQMRYLNCSFSISRATGRLCGITRVSLKKRVCIFLNPVLLSHLPSSSRSLMSPGVSQESEKLESVNAELKAQIEELKNEK
QHLIYMLNLHRPTCIVRAQNGRTPEDERILFIQQIKEGTLQS*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004300396 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ATF3 CLINVAR
OMIM 603148 CLINVAR