Isoform Positions

Isoform Protein Position Transcript Position Chromosomal Position (HG38) Chromosomal Position (HG19)
IC1601248259;48260;48261 chr2:178616855;178616854;178616853chr2:179481582;179481581;179481580
N2AB1437143336;43337;43338 chr2:178616855;178616854;178616853chr2:179481582;179481581;179481580
N2A1344440555;40556;40557 chr2:178616855;178616854;178616853chr2:179481582;179481581;179481580
N2B694721064;21065;21066 chr2:178616855;178616854;178616853chr2:179481582;179481581;179481580
Novex-1707221439;21440;21441 chr2:178616855;178616854;178616853chr2:179481582;179481581;179481580
Novex-2713921640;21641;21642 chr2:178616855;178616854;178616853chr2:179481582;179481581;179481580
Novex-3NoneNone chr2:Nonechr2:None

Information

  • RefSeq wild type amino acid: K
  • RefSeq wild type transcript codon: AAG
  • RefSeq wild type template codon: TTC
  • Domain: Ig-109
  • Domain position: 45
  • Structural Position: 125
  • Q(SASA): 0.4993
  • 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
K/T rs2057430031 None 0.023 N 0.174 0.192 0.26169431596 gnomAD-3.1.2 6.58E-06 None None None None N None 0 0 0 0 0 None 0 0 0 2.07125E-04 0
K/T rs2057430031 None 0.023 N 0.174 0.192 0.26169431596 gnomAD-4.0.0 6.58215E-06 None None None None N None 0 0 None 0 0 None 0 0 0 2.07125E-04 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
K/A 0.2969 likely_benign 0.3534 ambiguous -0.5 Destabilizing 0.495 N 0.313 neutral None None None None N
K/C 0.6335 likely_pathogenic 0.6836 pathogenic -0.635 Destabilizing 0.995 D 0.327 neutral None None None None N
K/D 0.3655 ambiguous 0.4286 ambiguous -0.168 Destabilizing 0.543 D 0.399 neutral None None None None N
K/E 0.1369 likely_benign 0.1666 benign -0.052 Destabilizing 0.006 N 0.091 neutral N 0.480442911 None None N
K/F 0.743 likely_pathogenic 0.7754 pathogenic -0.208 Destabilizing 0.893 D 0.39 neutral None None None None N
K/G 0.4359 ambiguous 0.4791 ambiguous -0.847 Destabilizing 0.704 D 0.425 neutral None None None None N
K/H 0.2338 likely_benign 0.2577 benign -1.041 Destabilizing 0.944 D 0.354 neutral None None None None N
K/I 0.3044 likely_benign 0.3647 ambiguous 0.393 Stabilizing 0.543 D 0.453 neutral None None None None N
K/L 0.3515 ambiguous 0.405 ambiguous 0.393 Stabilizing 0.329 N 0.332 neutral None None None None N
K/M 0.2218 likely_benign 0.2647 benign 0.047 Stabilizing 0.065 N 0.18 neutral D 0.565344046 None None N
K/N 0.2069 likely_benign 0.2534 benign -0.527 Destabilizing 0.642 D 0.308 neutral D 0.562855301 None None N
K/P 0.897 likely_pathogenic 0.9019 pathogenic 0.125 Stabilizing 0.828 D 0.401 neutral None None None None N
K/Q 0.1153 likely_benign 0.1306 benign -0.52 Destabilizing 0.023 N 0.189 neutral N 0.48735299 None None N
K/R 0.0886 likely_benign 0.0905 benign -0.531 Destabilizing 0.473 N 0.301 neutral N 0.511021556 None None N
K/S 0.2938 likely_benign 0.3443 ambiguous -1.096 Destabilizing 0.329 N 0.282 neutral None None None None N
K/T 0.1266 likely_benign 0.1581 benign -0.775 Destabilizing 0.023 N 0.174 neutral N 0.49683401 None None N
K/V 0.256 likely_benign 0.3134 benign 0.125 Stabilizing 0.013 N 0.137 neutral None None None None N
K/W 0.7867 likely_pathogenic 0.7986 pathogenic -0.147 Destabilizing 0.995 D 0.334 neutral None None None None N
K/Y 0.5944 likely_pathogenic 0.6326 pathogenic 0.14 Stabilizing 0.981 D 0.37 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.