Variant ID: 19-57335986-TT-GC

NM_001146184.1(PEG3):c.37_38delinsGC;(p.Lys13Ala)

This variant was identified in 1 publication




Publications:


Investigating PKA-RII specificity using analogs of the PKA:AKAP peptide inhibitor STAD-2.

Bioorganic & Medicinal Chemistry
NG Bendzunas, S Dörfler, K Autenrieth, D Bertinetti, EMF Machal, EJ Kennedy, FW Herberg
Publication Date: 2018-03-15

Variant appearance in text: PEG3: K13A
PubMed Link: 29449124
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000221722.5 c.-150-192_-150-191delinsGC - intron_variant - 2/10
ENST00000326441.9 c.37_38delinsGC p.Lys13Ala missense_variant 4/10 -
ENST00000391708.3 c.-237-105_-237-104delinsGC - intron_variant - 3/11
ENST00000423103.2 c.37_38delinsGC p.Lys13Ala missense_variant 3/9 -
ENST00000593695.1 c.-150-192_-150-191delinsGC - intron_variant - 2/8
ENST00000593711.1 c.-150-192_-150-191delinsGC - intron_variant - 2/10
ENST00000594389.1 c.37_38delinsGC p.Lys13Ala missense_variant 3/3 -
ENST00000594706.1 n.442-192_442-191delinsGC - intron_variant,non_coding_transcript_variant - 4/4
ENST00000595671.1 c.-150-192_-150-191delinsGC - intron_variant,NMD_transcript_variant - 1/11
ENST00000596261.1 n.421-192_421-191delinsGC - intron_variant,non_coding_transcript_variant - 4/4
ENST00000597281.1 c.-150-192_-150-191delinsGC - intron_variant,NMD_transcript_variant - 2/11
ENST00000598410.1 c.-150-192_-150-191delinsGC - intron_variant - 2/8
ENST00000599534.1 c.37_38delinsGC p.Lys13Ala missense_variant 1/7 -
ENST00000599577.1 c.37_38delinsGC p.Lys13Ala missense_variant 3/9 -
ENST00000599935.1 c.-237-105_-237-104delinsGC - intron_variant - 3/11
ENST00000600833.1 c.-342_-341delinsGC - 5_prime_UTR_variant 1/6 -
ENST00000601070.1 c.-150-192_-150-191delinsGC - intron_variant - 2/10
NM_001146184.2 c.37_38delinsGC p.Lys13Ala missense_variant 3/9 -
NM_001146185.2 c.-150-192_-150-191delinsGC - intron_variant - 2/8
NM_001146187.2 c.-150-192_-150-191delinsGC - intron_variant - 2/8
NM_001146326.2 c.-150-192_-150-191delinsGC - intron_variant - 3/11
NM_001146327.1 c.-237-105_-237-104delinsGC - intron_variant - 3/11
NM_001369717.1 c.37_38delinsGC p.Lys13Ala missense_variant 3/9 -
NM_001369718.1 c.37_38delinsGC p.Lys13Ala missense_variant 4/10 -
NM_001369719.1 c.37_38delinsGC p.Lys13Ala missense_variant 4/9 -
NM_001369720.1 c.-150-192_-150-191delinsGC - intron_variant - 5/11
NM_001369721.1 c.-237-105_-237-104delinsGC - intron_variant - 2/8
NM_001369722.1 c.-150-192_-150-191delinsGC - intron_variant - 3/9
NM_001369723.1 c.-150-192_-150-191delinsGC - intron_variant - 4/10
NM_001369724.1 c.-150-192_-150-191delinsGC - intron_variant - 5/11
NM_001369725.1 c.-150-192_-150-191delinsGC - intron_variant - 2/8
NM_001369726.1 c.-150-192_-150-191delinsGC - intron_variant - 4/10
NM_001369727.1 c.-235-107_-235-106delinsGC - intron_variant - 3/9
NM_001369728.1 c.-150-192_-150-191delinsGC - intron_variant - 4/10
NM_001369729.1 c.-237-105_-237-104delinsGC - intron_variant - 3/9
NM_001369730.1 c.-150-192_-150-191delinsGC - intron_variant - 3/9
NM_001369731.1 c.-150-192_-150-191delinsGC - intron_variant - 4/10
NM_001369732.1 c.-237-105_-237-104delinsGC - intron_variant - 3/9
NM_001369733.1 c.-150-192_-150-191delinsGC - intron_variant - 2/8
NM_001369734.1 c.-150-192_-150-191delinsGC - intron_variant - 3/8
NM_001369735.1 c.-150-192_-150-191delinsGC - intron_variant - 2/7
NM_001369736.1 c.-237-105_-237-104delinsGC - intron_variant - 2/7
NM_001369737.1 c.-150-192_-150-191delinsGC - intron_variant - 3/8
NM_001369738.1 c.-150-192_-150-191delinsGC - intron_variant - 4/9
NM_001369739.1 c.-150-192_-150-191delinsGC - intron_variant - 3/9
NM_001369770.1 c.-237-105_-237-104delinsGC - intron_variant - 3/11
NM_001369771.1 c.-150-192_-150-191delinsGC - intron_variant - 3/11
NM_001369772.1 c.-150-192_-150-191delinsGC - intron_variant - 2/10
NM_001369773.1 c.-150-192_-150-191delinsGC - intron_variant - 2/11
NM_001369774.1 c.-150-192_-150-191delinsGC - intron_variant - 2/11
NM_006210.3 c.37_38delinsGC p.Lys13Ala missense_variant 4/10 -
NM_015363.5 c.-150-192_-150-191delinsGC - intron_variant - 2/10
NR_163140.1 n.309-192_309-191delinsGC - intron_variant,non_coding_transcript_variant - 3/12
NR_163141.1 n.233-192_233-191delinsGC - intron_variant,non_coding_transcript_variant - 2/12
NR_163142.1 n.364-192_364-191delinsGC - intron_variant,non_coding_transcript_variant - 3/13
NR_163143.1 n.431_432delinsGC - non_coding_transcript_exon_variant 4/13 -