RGD:8635774 Rat Genome Database

RGD:8635774 Rat Genome Database

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Variant: RGD:8635774 - Homo sapiens

RGD ID:

8635774

ClinVar ID:

CV90997

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

Reference Nucleotide:

G

Variant Nucleotide:

A

Position

Assembly	Chr	Position
GRCh37	16	30,904,000
GRCh38	16	30,892,679

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

ClinVar Data

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NC_000016.10:g.30892679C>T NC_000016.9:g.30904000C>T NR_031576.1:c.1-u1224C>T NM_001330.2:c.-37-u3928C>T More...		2kb upstream variant\|intron variant\|missense variant	not provided	Malignant melanoma, somatic

Variant Details

Variant Transcripts

Gene Symbol:	BCL7C
Accession:	XM_047434897
Location:	EXON
Amino Acid Prediction:	G to G (synonymous)
Amino Acid Position:	80

Amino Acid Sequence (Calculated using NCBI transcript definition)
MAGRTVRAETRSRAKDDIKKVMATIEKVRRWEKRWVTVGDTSLRIFKWVPVVDPQEEMRTATRVSIRKVPCKRAQSPVLG APPSPAALCHLPDPQKGSLRRLSPHGWAKREVGPDPGGITAGSTDEPPMLTKEEPVPELLEAETMEMMLDKKQIQAIFLF ELKMGHKAVETLRNINNTLGPGTANEHIVQWWFKKFCKEDKSLEDEKHSVWPSEVDNDQLKALIEADPVKTTQEVAQELN HRPFYGRLAFEANWKGEKAQ*

Gene Symbol:	BCL7C
Accession:	XM_047434898
Location:	EXON
Amino Acid Prediction:	G to C (nonsynonymous)
Amino Acid Position:	51

Amino Acid Sequence (Calculated using NCBI transcript definition)
MGEAMGDCGRHFPSYLQVGASGGSPGGDENSNQSFHSEGSLQKGTEPSPGCTPQPSRPVSPAGPPEGVPEEAQPPRLGQE RDPGGITAGSTDEPPMLTKEEPVPELLEAETMEMMLDKKQIQAIFLFELKMGHKAVETLRNINNTLGPGTANEHIVQWWF KKFCKEDKSLEDEKHSVWPSEVDNDQLKALIEADPVKTTQEVAQELNHRPFYGRLAFEANWKGEKAQ*

Gene Symbol:	BCL7C
Accession:	XM_047434899
Location:	EXON
Amino Acid Prediction:	G to G (synonymous)
Amino Acid Position:	80

Amino Acid Sequence (Calculated using NCBI transcript definition)
MAGRTVRAETRSRAKDDIKKVMATIEKVRRWEKRWVTVGDTSLRIFKWVPVVDPQEEMRTATRVSIRKVPCKRAQSPVLG APPSPAALCHLPDPQKGSLRRLSPHGWAKREVGPDPGGITAGSTDEPPMLTKEEPVPELLEAEAPEAYPVFEPVPPVPEA AQGDTEDSEGAPPLKRICPNAPDP*

Gene Symbol:	BCL7C
Accession:	NM_004765
Location:	EXON
Amino Acid Prediction:	G to C (nonsynonymous)
Amino Acid Position:	117

Amino Acid Sequence (Calculated using NCBI transcript definition)
MAGRTVRAETRSRAKDDIKKVMATIEKVRRWEKRWVTVGDTSLRIFKWVPVVDPQEEERRRAGGGAERSRGRERRGRGAS PRGGGPLILLDLNDENSNQSFHSEGSLQKGTEPSPGCTPQPSRPVSPAGPPEGVPEEAQPPRLGQERDPGGITAGSTDEP PMLTKEEPVPELLEAEAPEAYPVFEPVPPVPEAAQGDTEDSEGAPPLKRICPNAPDP*

Gene Symbol:	BCL7C
Accession:	NM_001286526
Location:	EXON
Amino Acid Prediction:	G to C (nonsynonymous)
Amino Acid Position:	117

Amino Acid Sequence (Calculated using NCBI transcript definition)
MAGRTVRAETRSRAKDDIKKVMATIEKVRRWEKRWVTVGDTSLRIFKWVPVVDPQEEERRRAGGGAERSRGRERRGRGAS PRGGGPLILLDLNDENSNQSFHSEGSLQKGTEPSPGCTPQPSRPVSPAGPPEGVPEEAQPPRLGQERDPGGITAGSTDEP PMLTKEEPVPELLEAEDSGVRMTRRALHEKGLKTEPLRRLLPRRGLRTNVRPSSMAVPDTRAPGGGSKAPRAPRTIPQGK GR*

Gene Symbol:	BCL7C
Accession:	XM_047434900
Location:	EXON
Amino Acid Prediction:	G to G (synonymous)
Amino Acid Position:	80

Amino Acid Sequence (Calculated using NCBI transcript definition)
MAGRTVRAETRSRAKDDIKKVMATIEKVRRWEKRWVTVGDTSLRIFKWVPVVDPQEEMRTATRVSIRKVPCKRAQSPVLG APPSPAALCHLPDPQKGSLRRLSPHGWAKREIPGA*

Gene Symbol:	BCL7C
Accession:	XM_011545980
Location:	EXON
Amino Acid Prediction:	G to C (nonsynonymous)
Amino Acid Position:	117

Amino Acid Sequence (Calculated using NCBI transcript definition)
MAGRTVRAETRSRAKDDIKKVMATIEKVRRWEKRWVTVGDTSLRIFKWVPVVDPQEEERRRAGGGAERSRGRERRGRGAS PRGGGPLILLDLNDENSNQSFHSEGSLQKGTEPSPGCTPQPSRPVSPAGPPEGVPEEAQPPRLGQERDPGGITAGSTDEP PMLTKEEPVPELLEAETMEMMLDKKQIQAIFLFELKMGHKAVETLRNINNTLGPGTANEHIVQWWFKKFCKEDKSLEDEK HSVWPSEVDNDQLKALIEADPVKTTQEVAQELNHRPFYGRLAFEANWKGEKAQ*

Gene Symbol:	BCL7C
Accession:	XM_047434896
Location:	EXON
Amino Acid Prediction:	G to C (nonsynonymous)
Amino Acid Position:	117

Amino Acid Sequence (Calculated using NCBI transcript definition)
MAGRTVRAETRSRAKDDIKKVMATIEKVRRWEKRWVTVGDTSLRIFKWVPVVDPQEEERRRAGGGAERSRGRERRGRGAS PRGGGPLILLDLNDENSNQSFHSEGSLQKGTEPSPGCTPQPSRPVSPAGPPEGVPEEAQPPRLGQERDPGGITAGSTDEP PMLTKEEPVPELLEAERRGLTILPRLVLNSWAQAIHLPLPPKVLGLQTMEMMLDKKQIQAIFLFELKMGHKAVETLRNIN NTLGPGTANEHIVQWWFKKFCKEDKSLEDEKHSVWPSEVDNDQLKALIEADPVKTTQEVAQELNHRPFYGRLAFEANWKG EKAQ*

Gene Symbol:	MIR762HG
Accession:	NR_110941
Location:	INTRON;NON-CODING

Gene Symbol:	MIR762HG
Accession:	NR_110940
Location:	INTRON;NON-CODING

Gene Symbol:	MIR762HG
Accession:	NR_110942
Location:	INTRON;NON-CODING

Variant Samples