RGD:8626531 Rat Genome Database

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Variant: RGD:8626531 -  Homo sapiens

RGD ID: 8626531
ClinVar ID: CV81675
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DLC1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 13,072,181
GRCh38 8 13,214,672
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_182643.2:c.1348+90597C>T
NG_015998.1:g.305249C>T
NC_000008.11:g.13214672G>A
NC_000008.10:g.13072181G>A
More... 		intron|intron variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:DLC1
Accession:NM_001413127
Location:5UTRS;INTRON

Gene Symbol:DLC1
Accession:NM_001413128
Location:5UTRS;INTRON

Gene Symbol:DLC1
Accession:NM_001413133
Location:5UTRS;INTRON

Gene Symbol:DLC1
Accession:NM_001348083
Location:5UTRS;INTRON

Gene Symbol:DLC1
Accession:NM_001413131
Location:5UTRS;INTRON

Gene Symbol:DLC1
Accession:NM_001413126
Location:5UTRS;INTRON

Gene Symbol:DLC1
Accession:NM_001348082
Location:5UTRS;INTRON

Gene Symbol:DLC1
Accession:NM_001413125
Location:EXON
Amino Acid Prediction: P to L (nonsynonymous)
Amino Acid Position: 485
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MSVAIRKRSWEEHVTHWMGQPFNSDDRNTACHHGLVADSLQASMEKDATLNVDRKEKCVSLPDCCHGSELRDFPGRPMGH
LSKDVDENDSHEGEDQFLSLEASTETLVHVSDEDNNADLCLTDDKQVLNTQGQKTSGQHMIQGAGSLEKALPIIQSNQVS
SNSWGIAGETELALVKESGERKVTDSISKSLELCNEISLSEIKDAPKVNAVDTLNVKDIAPEKQLLNSAVIAQQRRKPDP
PKDENERSTCNVVQNEFLDTPCTNRGLPLLKTDFGSCLLQPPSCPNGMSAENGLEKSGFSQHQNKSPPKVKAEDGMQCLQ
LKETLATQEPTDNQVRLRKRKEIREDRDRARLDSMVLLIMKLDQLDQDIENALSTSSSPSGTPTNLRRHVPDLESGSESG
ADTISVNQTRVNLSSDTESTDLPSSTPVANSGTKPKTTAIQGISEKEKAAAVKSVKLEVDEDKSTKGSNFSNSEVAIGLS
PYTFLQKRLFHVAGEENIT*

Gene Symbol:DLC1
Accession:NM_001413134
Location:EXON
Amino Acid Prediction: P to L (nonsynonymous)
Amino Acid Position: 81
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGDPKAHVMARPLRAPLRRSFSDHIRDSTARALDVIWKNTRDRRLAAVKSVKLEVDEDKSTKGSNFSNSEVAIGLSPYTF
LQKRLFHVAGEENIT*

Gene Symbol:DLC1
Accession:NM_001413129
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001413138
Location:INTRON

Gene Symbol:DLC1
Accession:NM_006094
Location:INTRON

Gene Symbol:DLC1
Accession:NM_024767
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001316668
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001348081
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001413139
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001413130
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001413135
Location:INTRON

Gene Symbol:DLC1
Accession:NM_182643
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001164271
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001413132
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001413136
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001413137
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001413140
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001413124
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:DLC1
Accession:NM_001348084
Location:INTRON

Variant Samples