Isoform Positions

Isoform Protein Position Transcript Position Chromosomal Position (HG38) Chromosomal Position (HG19)
IC33630101113;101114;101115 chr2:178535727;178535726;178535725chr2:179400454;179400453;179400452
N2AB3198996190;96191;96192 chr2:178535727;178535726;178535725chr2:179400454;179400453;179400452
N2A3106293409;93410;93411 chr2:178535727;178535726;178535725chr2:179400454;179400453;179400452
N2B2456573918;73919;73920 chr2:178535727;178535726;178535725chr2:179400454;179400453;179400452
Novex-12469074293;74294;74295 chr2:178535727;178535726;178535725chr2:179400454;179400453;179400452
Novex-22475774494;74495;74496 chr2:178535727;178535726;178535725chr2:179400454;179400453;179400452
Novex-3NoneNone chr2:Nonechr2:None

Information

  • RefSeq wild type amino acid: Q
  • RefSeq wild type transcript codon: CAG
  • RefSeq wild type template codon: GTC
  • Domain: Ig-159
  • Domain position: 35
  • Structural Position: 49
  • Q(SASA): 0.238
  • Predicted PPI site: N

Reported SAVs

SNV RS
DUET
PolyPhen-2
Condel
Rhapsody
REVEL
MVP
Source
MAF
Disease
Zygosity
Site annotation
mCSM PPI
Predicted PPI site
Comments
AFR
AMR
AMS
ASJ
EAS
EUR
FIN
MDE
NFE
SAS
OTH
Q/L None None 0.997 N 0.643 0.504 0.352048277211 gnomAD-4.0.0 1.59138E-06 None None None None N None 0 0 None 0 0 None 0 0 0 0 3.02425E-05

Saturation Mutagenesis

SAV
AlphaMissense (IC)
AlphaMissense Class (IC)
AlphaMissense (N2AB)
AlphaMissense Class (N2AB)
mCSM
mCSM class
PolyPhen-2
PolyPhen-2 Class
Rhapsody
Rhapsody Class
Condel
Condel Score
Site annotation
mCSM PPI
Predicted PPI site
Q/A 0.8105 likely_pathogenic 0.7675 pathogenic -0.784 Destabilizing 0.999 D 0.553 neutral None None None None N
Q/C 0.9813 likely_pathogenic 0.9685 pathogenic -0.271 Destabilizing 1.0 D 0.764 deleterious None None None None N
Q/D 0.9855 likely_pathogenic 0.977 pathogenic -0.98 Destabilizing 0.997 D 0.501 neutral None None None None N
Q/E 0.4575 ambiguous 0.3403 ambiguous -0.802 Destabilizing 0.993 D 0.407 neutral N 0.441239021 None None N
Q/F 0.9777 likely_pathogenic 0.9634 pathogenic -0.307 Destabilizing 1.0 D 0.775 deleterious None None None None N
Q/G 0.8703 likely_pathogenic 0.8404 pathogenic -1.202 Destabilizing 0.999 D 0.643 neutral None None None None N
Q/H 0.8897 likely_pathogenic 0.8228 pathogenic -0.947 Destabilizing 0.999 D 0.725 prob.delet. N 0.480469413 None None N
Q/I 0.9066 likely_pathogenic 0.8602 pathogenic 0.321 Stabilizing 0.999 D 0.779 deleterious None None None None N
Q/K 0.5734 likely_pathogenic 0.4292 ambiguous -0.352 Destabilizing 0.997 D 0.498 neutral N 0.407683808 None None N
Q/L 0.6766 likely_pathogenic 0.5987 pathogenic 0.321 Stabilizing 0.997 D 0.643 neutral N 0.435675699 None None N
Q/M 0.7553 likely_pathogenic 0.6978 pathogenic 0.664 Stabilizing 0.999 D 0.729 prob.delet. None None None None N
Q/N 0.8895 likely_pathogenic 0.8567 pathogenic -1.075 Destabilizing 0.999 D 0.661 neutral None None None None N
Q/P 0.9972 likely_pathogenic 0.9965 pathogenic -0.017 Destabilizing 0.999 D 0.779 deleterious N 0.452703146 None None N
Q/R 0.6238 likely_pathogenic 0.4913 ambiguous -0.406 Destabilizing 0.995 D 0.489 neutral N 0.427693721 None None N
Q/S 0.7858 likely_pathogenic 0.749 pathogenic -1.254 Destabilizing 0.999 D 0.486 neutral None None None None N
Q/T 0.7383 likely_pathogenic 0.6823 pathogenic -0.866 Destabilizing 0.993 D 0.689 prob.neutral None None None None N
Q/V 0.8346 likely_pathogenic 0.7851 pathogenic -0.017 Destabilizing 0.998 D 0.701 prob.neutral None None None None N
Q/W 0.9844 likely_pathogenic 0.9711 pathogenic -0.19 Destabilizing 1.0 D 0.76 deleterious None None None None N
Q/Y 0.9663 likely_pathogenic 0.9373 pathogenic 0.087 Stabilizing 1.0 D 0.789 deleterious None None None None N

Titin has multiple isoforms, the longest being the theoretical IC (inferred complete) isoform which contains all 363 in-frame titin exons. Here all isoform positions have been mapped onto the IC sequence, with an exception being the C-terminal of the much shorter novex-3 isoform. This contains the out of frame exon 48 which cannot be mapped to the other isoforms.