ENST00000420605.7 NR2C2AP

Information
Transcript ID
ENST00000420605.7
Genome
hg38
Position
chr19:19,201,416-19,203,357
Strand
-
CDS length
504
Amino acid length
168
Gene symbol
NR2C2AP
Gene type
protein-coding
Gene description
nuclear receptor 2C2 associated protein
Gene Entrez Gene ID
126382
Variants

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Target data :
MGeND data only
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
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Target data :
MGeND data only
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Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
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Target data :
MGeND data only
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Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Exon
Exon number Start Stop
6 19,201,416 19,201,563
5 19,201,931 19,202,041
4 19,202,331 19,202,398
3 19,202,470 19,202,575
2 19,202,791 19,202,881
1 19,203,023 19,203,357
CDS
Exon number Type Start Stop
6 CDS 19,201,474 19,201,563
5 CDS 19,201,931 19,202,041
4 CDS 19,202,331 19,202,398
3 CDS 19,202,470 19,202,575
2 CDS 19,202,791 19,202,881
1 CDS 19,203,023 19,203,060
Other genome
Genome Chromosome Start End Links
hg19 chr19 19,312,225 19,314,166 Link
CDS sequence
ATGACCCACTCTTTGGTTTGTCCAGAGACAGTGAGCAGGGTGAGTTCAGTGCTGAATCGCAACACTCGGCAGTTTGGAAAAAAACATCTTTTCGACCAGGATGAGGAGACATGTTGGAACTCAGACCAGGGCCCCTCCCAGTGGGTGACGCTGGAGTTTCCCCAGCTCATCCGTGTCTCCCAGCTGCAGATCCAGTTTCAGGGTGGCTTCTCCAGTCGCCGGGGCTGCCTGGAAGGTTCACAGGGCACTCAGGCTCTCCACAAGATTGTAGATTTCTACCCTGAGGACAACAACTCGCTTCAGACTTTCCCCATACCAGCTGCTGAAGTGGACCGGCTGAAGGTGACGTTTGAGGATGCCACTGACTTTTTTGGCCGTGTGGTCATCTACCACCTGCGGGTGCTTGGGGAGAAGGGGACAAACAGGGACCCTTGCAGAGACCTGCATTACAGAGCAAAGCTGGGAGAACCGAGGACTCACCCCAGGAACCTCAACTTCCCCTAA
Amino sequence
MTHSLVCPETVSRVSSVLNRNTRQFGKKHLFDQDEETCWNSDQGPSQWVTLEFPQLIRVSQLQIQFQGGFSSRRGCLEGSQGTQALHKIVDFYPEDNNSLQTFPIPAAEVDRLKVTFEDATDFFGRVVIYHLRVLGEKGTNRDPCRDLHYRAKLGEPRTHPRNLNFP*