Isoform Positions

Isoform Protein Position Transcript Position Chromosomal Position (HG38) Chromosomal Position (HG19)
IC1438143366;43367;43368 chr2:178632990;178632989;178632988chr2:179497717;179497716;179497715
N2AB1274038443;38444;38445 chr2:178632990;178632989;178632988chr2:179497717;179497716;179497715
N2A1181335662;35663;35664 chr2:178632990;178632989;178632988chr2:179497717;179497716;179497715
N2B531616171;16172;16173 chr2:178632990;178632989;178632988chr2:179497717;179497716;179497715
Novex-1544116546;16547;16548 chr2:178632990;178632989;178632988chr2:179497717;179497716;179497715
Novex-2550816747;16748;16749 chr2:178632990;178632989;178632988chr2:179497717;179497716;179497715
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-94
  • Domain position: 63
  • Structural Position: 145
  • Q(SASA): 0.277
  • 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/E rs754568652 0.077 0.002 N 0.124 0.112 0.128392430309 gnomAD-2.1.1 4.03E-06 None None None None N None 0 0 None 0 5.6E-05 None 0 None 0 0 0
Q/E rs754568652 0.077 0.002 N 0.124 0.112 0.128392430309 gnomAD-4.0.0 1.59264E-06 None None None None N None 0 0 None 0 2.78071E-05 None 0 0 0 0 0
Q/L rs1433049624 0.325 0.011 N 0.403 0.124 0.192905019026 gnomAD-2.1.1 4.03E-06 None None None None N None 6.46E-05 0 None 0 0 None 0 None 0 0 0
Q/L rs1433049624 0.325 0.011 N 0.403 0.124 0.192905019026 gnomAD-4.0.0 1.3689E-06 None None None None N None 5.98158E-05 0 None 0 0 None 0 0 0 0 0

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 0.2392 likely_benign 0.1972 benign -0.532 Destabilizing 0.006 N 0.251 neutral None None None None N
Q/C 0.5976 likely_pathogenic 0.5468 ambiguous 0.178 Stabilizing 0.747 D 0.481 neutral None None None None N
Q/D 0.3044 likely_benign 0.2595 benign -0.333 Destabilizing 0.015 N 0.196 neutral None None None None N
Q/E 0.0856 likely_benign 0.0785 benign -0.305 Destabilizing 0.002 N 0.124 neutral N 0.433406748 None None N
Q/F 0.6529 likely_pathogenic 0.5935 pathogenic -0.493 Destabilizing 0.204 N 0.629 neutral None None None None N
Q/G 0.2799 likely_benign 0.2257 benign -0.818 Destabilizing 0.015 N 0.33 neutral None None None None N
Q/H 0.1706 likely_benign 0.154 benign -0.792 Destabilizing None N 0.111 neutral N 0.423835432 None None N
Q/I 0.391 ambiguous 0.3667 ambiguous 0.163 Stabilizing 0.068 N 0.591 neutral None None None None N
Q/K 0.0679 likely_benign 0.0674 benign -0.224 Destabilizing None N 0.06 neutral N 0.372394702 None None N
Q/L 0.141 likely_benign 0.1266 benign 0.163 Stabilizing 0.011 N 0.403 neutral N 0.432205437 None None N
Q/M 0.3759 ambiguous 0.3422 ambiguous 0.677 Stabilizing 0.439 N 0.327 neutral None None None None N
Q/N 0.2281 likely_benign 0.201 benign -0.638 Destabilizing 0.015 N 0.231 neutral None None None None N
Q/P 0.1846 likely_benign 0.1723 benign -0.038 Destabilizing 0.052 N 0.48 neutral N 0.436137475 None None N
Q/R 0.084 likely_benign 0.0791 benign -0.109 Destabilizing None N 0.05 neutral N 0.336037062 None None N
Q/S 0.2119 likely_benign 0.1785 benign -0.667 Destabilizing 0.015 N 0.161 neutral None None None None N
Q/T 0.1788 likely_benign 0.155 benign -0.458 Destabilizing 0.015 N 0.376 neutral None None None None N
Q/V 0.271 likely_benign 0.2415 benign -0.038 Destabilizing 0.035 N 0.515 neutral None None None None N
Q/W 0.5335 ambiguous 0.4671 ambiguous -0.4 Destabilizing 0.747 D 0.511 neutral None None None None N
Q/Y 0.4397 ambiguous 0.3817 ambiguous -0.182 Destabilizing 0.035 N 0.521 neutral 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.